| Tobias Gedde-Dahl | |
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Author network for Tobias Gedde-Dahl by COREMINE medical
Publications in press
Bortezomib consolidation after autologous stem cell transplantation in multiple myeloma: a Nordic Myeloma Study Group randomized phase III trial
Blood (in press)
PubMed 23616624
Impact of malignant stem cell burden on therapy outcome in newly diagnosed chronic myeloid leukemia patients
Leukemia (in press)
PubMed 23328954
Publications 2012
Ultra-short course sirolimus contributes to effective GVHD prophylaxis after reduced-intensity allogeneic hematopoietic cell transplantation
Bone Marrow Transplant, 47 (12), 1552-7
PubMed 22522568
BCR-ABL isoforms associated with intrinsic or acquired resistance to imatinib: more heterogeneous than just ABL kinase domain point mutations?
Med Oncol, 29 (1), 219-26
PubMed 21221851
Publications 2011
Targeted idiotype-fusion DNA vaccines for human multiple myeloma: preclinical testing
Eur J Haematol, 86 (5), 385-95
PubMed 21332794
Combination of pegylated IFN-?2b with imatinib increases molecular response rates in patients with low- or intermediate-risk chronic myeloid leukemia
Blood, 118 (12), 3228-35
PubMed 21685374
Publications 2010
Improved survival for multiple myeloma in denmark based on autologous stem cell transplantation and novel drug therapy in collaborative trials: analysis of accrual, prognostic variables, selection bias, and clinical behavior on survival in more than 1200 patients in trials of the nordic myeloma study group
Clin Lymphoma Myeloma Leuk, 10 (4), 290-6
PubMed 20709667
Publications 2009
APC mutation spectrum of Norwegian familial adenomatous polyposis families: high ratio of novel mutations
J Cancer Res Clin Oncol, 135 (10), 1463-70
PubMed 19444466
Chronic myelogenous leukemia with the e6a2 BCR-ABL and lacking imatinib response: presentation of two cases
Acta Haematol, 122 (1), 11-6
PubMed 19641300
Publications 2008
[Allogeneic stem cell transplantation in acute myelogenous leukemia]
Tidsskr Nor Laegeforen, 128 (15), 1681-2; author reply 1682
PubMed 18704137
[Allogeneic stem cell transplantation in adults with acute lymphoblastic leukaemia]
Tidsskr Nor Laegeforen, 128 (22), 2563-6
PubMed 19023351
Imatinib pharmacokinetics and its correlation with response and safety in chronic-phase chronic myeloid leukemia: a subanalysis of the IRIS study
Blood, 111 (8), 4022-8
PubMed 18256322
Publications 2007
Gene symbol: APC
Hum Genet, 121 (2), 288
PubMed 17598199
Congenital ichthyosis: mutations in ichthyin are associated with specific structural abnormalities in the granular layer of epidermis
J Med Genet, 44 (10), 615-20
PubMed 17557927
A VH4-34+ myeloma protein with weak autoreactivity
Haematologica, 92 (5), 690-3
PubMed 17488696
Treatment outcome in adults with acute lymphoblastic leukemia: 50% long-term disease-free survival
Leukemia, 21 (10), 2203-4
PubMed 17525727
Publications 2006
[Epidermolysis bullosa simplex Dowling-Meara]
Ugeskr Laeger, 168 (48), 4222-4
PubMed 17147951
Fibroblast heterogeneity in collagenolytic response to colchicine
Biochem Pharmacol, 71 (5), 574-83
PubMed 16378602
Publications 2005
Selecting and deselecting imatinib-resistant clones: observations made by longitudinal, quantitative monitoring of mutated BCR-ABL
Leukemia, 19 (12), 2159-65
PubMed 16224487
Publications 2004
Immunotherapy in multiple myeloma: Id-specific strategies suggested by studies in animal models
Cancer Immunol Immunother, 53 (9), 759-69
PubMed 15088126
[Treatment of T-cell prolymphocytic leukemia with monoclonal anti- CD52 antibody (alemtuzumab]
Tidsskr Nor Laegeforen, 124 (6), 768-70
PubMed 15039804
Assignment of the locus for ichthyosis prematurity syndrome to chromosome 9q33.3-34.13
J Med Genet, 41 (3), 208-12
PubMed 14985385
Life-long course and molecular characterization of the original Dutch family with epidermolysis bullosa simplex with muscular dystrophy due to a homozygous novel plectin point mutation
Acta Derm Venereol, 84 (2), 124-31
PubMed 15206692
Activated prothrombin complex concentrate (FEIBA) treatment during surgery in patients with inhibitors to FVIII/IX
Haemophilia, 10 (2), 174-8
PubMed 14962207
Publications 2003
Splice site and deletion mutations in keratin (KRT1 and KRT10) genes: unusual phenotypic alterations in Scandinavian patients with epidermolytic hyperkeratosis
J Invest Dermatol, 121 (5), 1013-20
PubMed 14708600
Publications 2002
A site-specific plectin mutation causes dominant epidermolysis bullosa simplex Ogna: two identical de novo mutations
J Invest Dermatol, 118 (1), 87-93
PubMed 11851880
Protein C deficiency caused by homozygosity for a novel PROC D180G mutation--in vitro expression and structural analysis of the mutation
Thromb Haemost, 88 (4), 632-8
PubMed 12362235
Genotype-phenotype relationships in Berardinelli-Seip congenital lipodystrophy
J Med Genet, 39 (10), 722-33
PubMed 12362029
Publications 2001
[Genetic analysis in familial adenomatous polyposis]
Tidsskr Nor Laegeforen, 121 (1), 64-8
PubMed 12013617
Identification of the gene altered in Berardinelli-Seip congenital lipodystrophy on chromosome 11q13
Nat Genet, 28 (4), 365-70
PubMed 11479539
Generalized dystrophic epidermolysis bullosa: identification of a novel, homozygous glycine substitution, G2031S, in exon 73 of COL7A1 in monozygous triplets
Br J Dermatol, 144 (1), 151-7
PubMed 11167698
Familial/bilateral and sporadic testicular germ cell tumors show frequent genetic changes at loci with suggestive linkage evidence
Neoplasia, 3 (3), 196-203
PubMed 11494113
Truncated typeXVII collagen expression in a patient with non-herlitz junctional epidermolysis bullosa caused by a homozygous splice-site mutation
Lab Invest, 81 (6), 887-94
PubMed 11406649
Phenotypic/genotypic correlations in patients with epidermolytic hyperkeratosis and the effects of retinoid therapy on keratin expression
Acta Derm Venereol, 81 (3), 163-70
PubMed 11558869
Publications 2000
DXYS267: DYS393 and its X chromosome counterpart
Forensic Sci Int, 112 (2-3), 111-21
PubMed 10940596
Haplotype association and mutation analysis of the transglutaminase 1 gene for prenatal exclusion of lamellar ichthyosis
Prenat Diagn, 20 (2), 132-7
PubMed 10694685
Publications 1999
[Serotonin syndrome with fatal outcome caused by selective serotonin reuptake inhibitors]
Tidsskr Nor Laegeforen, 119 (5), 647-50
PubMed 10095385
Publications 1998
Comparisons of allele frequencies in three hyperpolymorphic STRs between Norwegian Saamis and the main population
INT CONGR SER, 1167, 395-397
Strong founder effect for a transglutaminase 1 gene mutation in lamellar ichthyosis and congenital ichthyosiform erythroderma from Norway
Eur J Hum Genet, 6 (6), 589-96
PubMed 9887377
Publications 1997
Plectin abnormality in epidermolysis bullosa simplex Ogna: non-responsiveness of basal keratinocytes to some anti-rat plectin antibodies
Exp Dermatol, 6 (1), 41-8
PubMed 9067706
Implications of intragenic marker homozygosity and haplotype sharing in a rare autosomal recessive disorder: the example of the collagen type XVII (COL17A1) locus in generalised atrophic benign epidermolysis bullosa
Hum Genet, 100 (2), 230-5
PubMed 9254855
Modulation of disease severity of dystrophic epidermolysis bullosa by a splice site mutation in combination with a missense mutation in the COL7A1 gene
Hum Mol Genet, 6 (7), 1125-35
PubMed 9215684
Publications 1996
Genetic analysis of a severe case of Dowling-Meara epidermolysis bullosa simplex
J Invest Dermatol, 106 (2), 327-34
PubMed 8601736
Genetics of the Berardinelli-Seip syndrome (congenital generalized lipodystrophy) in Norway: epidemiology and gene mapping. Berardinelli-Seip Study Group
Acta Paediatr Suppl, 413, 52-8
PubMed 8783773
Ex vivo ras peptide vaccination in patients with advanced pancreatic cancer: results of a phase I/II study
Int J Cancer, 65 (4), 450-3
PubMed 8621226
Generalized atrophic benign epidermolysis bullosa. Either 180-kd bullous pemphigoid antigen or laminin-5 deficiency
Arch Dermatol, 132 (2), 145-50
PubMed 8629821
On the genetics of hypodontia and microdontia: synergism or allelism of major genes in a family with six affected members
J Med Genet, 33 (2), 137-42
PubMed 8929951
The genetic basis of epidermolysis bullosa simplex with mottled pigmentation
Proc Natl Acad Sci U S A, 93 (17), 9079-84
PubMed 8799157
Publications 1995
Immunohistochemical and mutation analyses demonstrate that procollagen VII is processed to collagen VII through removal of the NC-2 domain
J Cell Biol, 131 (2), 551-9
PubMed 7593178
Report of the second international workshop on human chromosome 14 mapping 1994
Cytogenet Cell Genet, 69 (3-4), 159-74
PubMed 7698004
Genes and languages in Europe: an analysis of mitochondrial lineages
Genome Res, 5 (1), 42-52
PubMed 8717054
Publications 1994
A K-ras 13Gly-->Asp mutation is recognized by HLA-DQ7 restricted T cells in a patient with colorectal cancer. Modifying effect of DQ7 on established cancers harbouring this mutation?
Int J Cancer, 58 (4), 506-11
PubMed 7914513
p21-ras-peptide-specific T-cell responses in a patient with colorectal cancer. CD4+ and CD8+ T cells recognize a peptide corresponding to a common mutation (13Gly-->Asp)
Int J Cancer, 56 (1), 40-5
PubMed 7903287
Junctional epidermolysis bullosa inversa (locus EBR2A) assigned to 1q31 by linkage and association to LAMC1
Hum Mol Genet, 3 (8), 1387-91
PubMed 7987320
Growth inhibition of a colonic adenocarcinoma cell line (HT29) by T cells specific for mutant p21 ras
Cancer Immunol Immunother, 38 (2), 127-34
PubMed 8306368
T cell epitopes encompassing the mutational hot spot position 61 of p21 ras. Promiscuity in ras peptide binding to HLA
Eur J Immunol, 24 (2), 410-4
PubMed 7507844
Neonatal retention of type VII collagen, transient bullous dermolysis of the newborn and recessive epidermolysis bullosa dystrophica inversa
Br J Dermatol, 130 (5), 685-6
PubMed 8204486
Binding of ras oncogene peptides to purified HLA-DQ (alpha 1*0102, beta 1*0602) and -DR (alpha, beta 1*0101) molecules
Scand J Immunol, 40 (4), 468
PubMed 7939420
Binding of ras oncogene peptides to purified HLA-DQ(alpha 1*0102,beta 1*0602) and -DR(alpha,beta 1*0101) molecules
Scand J Immunol, 39 (6), 607-12
PubMed 8009176
Heterogeneity of severe dystrophic epidermolysis bullosa: overexpression of collagen VII by cutaneous cells from a patient with mutilating disease
J Invest Dermatol, 102 (2), 155-9
PubMed 8106746
Heterogeneity of T cells specific for a particular peptide/HLA-DQ complex
Hum Immunol, 39 (1), 61-8
PubMed 8181964
Keratinocytes from junctional epidermolysis bullosa do adhere and migrate on the basement membrane protein nicein through alpha 3 beta 1 integrin
Lab Invest, 71 (4), 567-74
PubMed 7967512
Publications 1993
Overlapping epitopes encompassing a point mutation (12 Gly-->Arg) in p21 ras can be recognized by HLA-DR, -DP and -DQ restricted T cells
Eur J Immunol, 23 (10), 2687-91
PubMed 7691613
T cell clones specific for p21 ras-derived peptides: characterization of their fine specificity and HLA restriction
Eur J Immunol, 23 (3), 754-60
PubMed 8449222
Oncogene-derived peptides: a new class of tumor rejection antigens?
Transplant Proc, 25 (1 Pt 2), 1385-6
PubMed 8442151
Studies of the T-cell receptors of T cells recognizing the same HLA molecule
Transplant Proc, 25 (1 Pt 1), 72
PubMed 8438455
Publications 1992
Anchoring fibrils, collagen VII, and neutral metalloproteases in recessive dystrophic epidermolysis bullosa inversa
J Invest Dermatol, 99 (5), 550-8
PubMed 1431215
Symposium on epidermolysis bullosa
J Med Genet, 29 (5), 354-5
PubMed 1349925
T-cell responses against products of oncogenes: generation and characterization of human T-cell clones specific for p21 ras-derived synthetic peptides
Hum Immunol, 33 (4), 266-74
PubMed 1639630
Memory T cells of a patient with follicular thyroid carcinoma recognize peptides derived from mutated p21 ras (Gln-->Leu61)
Int Immunol, 4 (11), 1331-7
PubMed 1282032
The gene encoding human transmembrane secretory component (locus PIGR) is linked to D1S58 on chromosome 1
Hum Genet, 90 (3), 215-9
PubMed 1487233
Linkage and association studies with C8A and C8B RFLPs on chromosome 1
Ann Hum Genet, 56 (Pt 3), 233-42
PubMed 1360193
Epidermolysis bullosa simplex: expression of gelatinase activity in cultured human skin fibroblasts
Biochem Genet, 30 (7-8), 401-20
PubMed 1445183
Publications 1991
The human genes for complement components 6 (C6) and 9 (C9) are closely linked on chromosome 5
J Med Genet, 28 (9), 587-90
PubMed 1683409
Publications 1990
Report of the committee on the genetic constitution of chromosome 14
Cytogenet Cell Genet, 55 (1-4), 183-8
PubMed 2073832
High-resolution karyotypes of eighteen Norwegian polyposis patients
Cancer Genet Cytogenet, 47 (1), 69-72
PubMed 2162732
Multiple RFLPs of human complement component nine (C9) detected by TaqI
Nucleic Acids Res, 18 (10), 3112
PubMed 1971940
Publications 1989
[A Norwegian polyposis family. From catastrophe to prevention]
Tidsskr Nor Laegeforen, 109 (7-8), 832-5
PubMed 2539657
[The polyposis project]
Nord Med, 104 (1), 12-5
PubMed 2536147
The genes for apolipoprotein all (APOA2) and the Duffy blood group (FY) are linked on chromosome 1 in man
Genomics, 4 (2), 169-73
PubMed 2500391
Collagenase expression in skin fibroblasts from families with recessive dystrophic epidermolysis bullosa
J Invest Dermatol, 92 (1), 82-5
PubMed 2535863
Publications 1988
International Nosology of Heritable Disorders of Connective Tissue, Berlin, 1986
Am J Med Genet, 29 (3), 581-94
PubMed 3287925
Report of the committee on the genetic constitution of chromosomes 14 and 15
Cytogenet Cell Genet, 49 (1-3), 90-3
PubMed 3203557
Hepatoblastoma and familial adenomatous polyposis
J Natl Cancer Inst, 80 (20), 1626-8
PubMed 2848134
[The polyposis project]
Tidsskr Nor Laegeforen, 108 (29), 2465-8
PubMed 2905084
VNTR (variable number of tandem repeats) markers show loss of chromosome 17p sequences in human colorectal carcinomas
Cytogenet Cell Genet, 48 (3), 167-9
PubMed 2906851
Restriction fragment length polymorphisms of the complement component C4 loci on chromosome 6: studies with emphasis on the determination of gene number
Ann Hum Genet, 52 (Pt 2), 77-84
PubMed 2907852
Publications 1987
The human gene map and genes expressed in the skin
Curr Probl Dermatol, 16, 45-64
PubMed 3556034
Epidermolysis bullosa syndromes
Curr Probl Dermatol, 16, 129-45
PubMed 3581883
The Kidd (JK) blood group locus assigned to chromosome 18 by close linkage to a DNA-RFLP
Hum Genet, 77 (3), 205-9
PubMed 2890568
Chromosome 13 instability and esterase D expression in an osteosarcoma cell line
Cancer Genet Cytogenet, 24 (2), 327-34
PubMed 2878716
Loss of one chromosome #13 during development of a polyposis tumor
Cancer Genet Cytogenet, 28 (2), 335-42
PubMed 2887278
Report of the committee on the genetic constitution of chromosomes 13, 14, 15 amd 16
Cytogenet Cell Genet, 46 (1-4), 213-41
PubMed 3507275
Publications 1986
Clinical heterogeneity in epidermolysis bullosa: speculations on causation and consequence for research
J Invest Dermatol, 86 (2), 91-3
PubMed 3745948
Very close linkage between D2S1 and ACP1 on chromosome 2p
Ann Hum Genet, 50 (Pt 4), 361-7
PubMed 3481680
The C8A and C8B loci are closely linked on chromosome 1
Ann Hum Genet, 50 (Pt 2), 139-44
PubMed 3435043
Confirmation of the close linkage between the loci for human apolipoproteins AI and AIV by the use of a cloned cDNA probe and two restriction site polymorphisms
Hum Genet, 72 (1), 68-71
PubMed 3002953
Gelatinase expression in generalized epidermolysis bullosa simplex fibroblasts
J Invest Dermatol, 87 (3), 326-9
PubMed 3016106
Publications 1985
Report of the Committee on the Genetic Constitution of Chromosomes 13, 14, 15 and 16
Cytogenet Cell Genet, 40 (1-4), 206-41
PubMed 3864595
Nomenclature Committee report: pepsinogens. Nomenclature Committee of Human Gene Mapping Conference
Prog Clin Biol Res, 173, 41-2
PubMed 3983197
On chromosome mapping of human pepsinogen gene loci
Prog Clin Biol Res, 173, 101-6
PubMed 3983190
Testicular neoplasms occurring in four brothers. A search for a genetic predisposition
Cancer, 55 (9), 2005-9
PubMed 2983872
Osteosarcoma and retinoblastoma: a shared chromosomal mechanism revealing recessive predisposition
Proc Natl Acad Sci U S A, 82 (18), 6216-20
PubMed 2994066
A structural locus for coagulation factor XIIIA (F13A) is located distal to the HLA region on chromosome 6p in man
Am J Hum Genet, 37 (1), 215-20
PubMed 2858156
Genetic polymorphism of complement component C8
Hum Genet, 70 (3), 211-6
PubMed 3879968
Publications 1984
The locus for apolipoprotein E (apoE) is close to the Lutheran (Lu) blood group locus on chromosome 19
Hum Genet, 67 (2), 178-82
PubMed 6745937
The locus for apolipoprotein CII is closely linked to the apolipoprotein E locus on chromosome 19 in man
Hum Genet, 67 (3), 309-12
PubMed 6088388
The two apolipoprotein loci apo A-I and apo A-IV are closely linked in man
Hum Genet, 68 (2), 181-4
PubMed 6500569
Publications 1983
Gene order and gene distances in the HLA region studied by the haplotype method
Ann Hum Genet, 47 (Pt 4), 285-92
PubMed 6418058
Genetic studies of an apoA-I lipoprotein variant
Hum Genet, 64 (4), 380-3
PubMed 6413385
Publications 1982
Final eradication of tuberculosis in Norway?
J Oslo City Hosp, 32 (9), 107-9
PubMed 7143132
The locus for apolipoprotein E (apoE) is linked to the complement component C3 (C3) locus on chromosome 19 in man
Hum Genet, 62 (3), 233-6
PubMed 7169215
Fibrinogen gamma chain locus is on chromosome 4 in man
Hum Genet, 61 (1), 24-6
PubMed 6957371
Workshop on mapping by classical methods
Prog Clin Biol Res, 103 Pt A, 141-4
PubMed 7163191
Publications 1981
Sixteen types of epidermolysis bullosa. On the clinical discrimination, therapy and prenatal diagnosis
Acta Derm Venereol Suppl (Stockh), 95, 74-87
PubMed 6953718
The Gm--Pi linkage heterogeneity in view of Pi M subtypes
Ann Hum Genet, 45 (Pt 2), 143-53
PubMed 6797346
C4 haplotype products and partial inhibition of anti-Rodgers sera
J Immunogenet, 8 (6), 485-91
PubMed 7334218
The ESD polymorphism: further studies of the ESD2 and ESD5 allele products
Hum Genet, 57 (4), 351-3
PubMed 7286974
Complement loci of the HLA complex. Studies on families with intra-HLA crossovers and haplotype associations
Hum Immunol, 2 (3), 247-54
PubMed 6455398
Publications 1980
Genetics of pepsinogen I
Ann Hum Genet, 43 (3), 199-212
PubMed 6767433
Genetic linkage relation to the pepsinogen Pg5 locus
Ann Hum Genet, 44 (Pt 2), 185-94
PubMed 7316469
Association between the electrophoretically-determined C4M haplotype product and partial inhibition of anti-Cha
J Immunogenet, 7 (4), 301-6
PubMed 6161195
Further investigations on the genetics of the C+ protein polymorphism
Immunobiology, 158 (1-2), 45-9
PubMed 7203519
Publications 1979
Epidermolysis bullosa simplex and mottled pigmentation: a new dominant syndrome. I. Clinical and histological features
Clin Genet, 15 (3), 228-38
PubMed 421361
The C4 system: formal and population genetics
Hum Genet, 50 (2), 187-92
PubMed 511133
Human complement C4 locus is duplicated on some chromosomes
Nature, 279 (5715), 736-7
PubMed 450123
Genetic linkage relations of the sixth component of complement (C6)
Hum Genet, 46 (2), 181-92
PubMed 422202
Publications 1978
Mapping with B-cell hybrids
Cytogenet Cell Genet, 22 (1-6), 661-5
PubMed 313313
Regional chromosome 12 mapping: information from a family with a (12;21) reciprocal translocation
Cytogenet Cell Genet, 22 (1-6), 478-81
PubMed 752526
Pepsinogens: new variant and linkage relationships to chromosome 6 markers
Cytogenet Cell Genet, 22 (1-6), 301-3
PubMed 752491
Genetic polymorphism of the second component of human complement (C2): presentation of a modified typing technique and data on C2 phenotype distribution, linkage genetics, and haplotype associations a Norwegian family material
Hum Genet, 42 (3), 301-5
PubMed 669711
Structural complement factor loci and the HLA region
Cytogenet Cell Genet, 22 (1-6), 421-7
PubMed 752517
Publications 1977
The role of human skin collagenase in epidermolysis bullosa
J Invest Dermatol, 68 (3), 119-24
PubMed 190326
HLA and epidermolysis bullosa
Arch Dermatol, 113 (12), 1722-3
PubMed 596909
Nonlinkage between C6 and chromosome 6 markers
Hum Genet, 37 (2), 125-9
PubMed 885533
The genetic polymorphism of the fourth component of human complement: methodological aspects and a presentation of linkage and association data relevant to its localization in the HLA region
J Exp Med, 146 (5), 1380-9
PubMed 925607
Publications 1976
Linkage data on 3q11 and 15ps fluorescence markers
Cytogenet Cell Genet, 16 (1-5), 275-6
PubMed 975889
Effect of age on the Gm:Pi linkage
Cytogenet Cell Genet, 16 (1-5), 298-301
PubMed 1086184
Effect of age on the gm:pi linkage
Birth Defects Orig Artic Ser, 12 (7), 298-301
PubMed 1088254
Chido blood group and the HLA region
Cytogenet Cell Genet, 16 (1-5), 307-10
PubMed 975894
Chido blood group and the HLA region
Birth Defects Orig Artic Ser, 12 (7), 307-10
PubMed 1024629
Rodgers blood group and the HLA region
Cytogenet Cell Genet, 16 (1-5), 311-2
PubMed 975896
Rodgers blood group and the HLA region
Birth Defects Orig Artic Ser, 12 (7), 311-2
PubMed 1024630
Rga (Rodgers) and the HLA region: linkage and associations
Tissue Antigens, 8 (2), 143-9
PubMed 968900
Ultrastructural studies in epidermolysis bullosa hereditaria. IV. Recessive dystrophic types with junctional blistering. (Infantile or Herlitz-Pearson type and adult type)
Arch Dermatol Res, 257 (1), 17-32
PubMed 1008602
Ultrastructural studies in epidermolysis bullosa hereditaria. II. Dominant dystrophic type of Cockayne and Touraine
Arch Dermatol Res, 255 (3), 285-95
PubMed 942257
Ultrastructural studies in epidermolysis bullosa hereditaria. III. Recessive dystrophic types with dermolytic blistering (Hallopeau-Siemens types and inverse type)
Arch Dermatol Res, 256 (2), 137-50
PubMed 962387
Localization of the human GLO gene locus
Hum Genet, 32 (3), 301-4
PubMed 939550
Bf locus and the HLA region
Cytogenet Cell Genet, 16 (1-5), 345-6
PubMed 975905
Bf locus and the HLA region
Birth Defects Orig Artic Ser, 12 (7), 345-6
PubMed 1024638
Genetic polymorphism of C4 in man and localisation of a structural C4 locus to the HLA gene complex of chromosome 6
Nature, 264 (5583), 253-4
PubMed 1088823
Publications 1975
The Gm-Pi linkage: a summary estimate
Cytogenet Cell Genet, 14 (3-6), 327-8
PubMed 53124
The Gm-Pi linkage: a summary estimate
Birth Defects Orig Artic Ser, 11 (3), 157-8
PubMed 54196
Improved estimate of the Gm-Pi linkage
Ann Hum Genet, 39 (1), 43-50
PubMed 810069
Ultrastructural studies in epidermolysis bullosa heriditaria. I. Dominant dystrophic type of Pasini
Arch Dermatol Forsch, 252 (3), 167-78
PubMed 1155959
The Bf locus in the HLA region of chromosome 6: linkage and association studies
Humangenetik, 30 (4), 291-6
PubMed 1218859
On the localization of the Gb locus within the MHS region of chromosome No. 6
Tissue Antigens, 5 (4), 257-61
PubMed 1154360
Linkage relations of the loci for the MN blood group and red cell acid phosphatase
Cytogenet Cell Genet, 14 (3-6), 446-50
PubMed 1192835
Linkage relations of the loci for the MN blood group and red cell acid phosphatase
Birth Defects Orig Artic Ser, 11 (3), 276-80
PubMed 1203495
Publications 1974
C3 polymorphism: genetic linkage relations
Clin Genet, 6 (1), 66-72
PubMed 4426132
Gpt-EBS1 linkage group. General linkage relations
Hum Hered, 24 (2), 178-85
PubMed 4425507
Publications 1973
Population structure in Norway. Inbreeding, distance and kinship
Hereditas, 73 (2), 211-32
PubMed 4713280
GPT--epidermolysis bullosa simplex (EBS Ogna) linkage in man
Hum Hered, 23 (3), 189-96
PubMed 4760576
Publications 1972
Autosomal linkage between the Gm and Pi loci in man
Ann Hum Genet, 35 (4), 393-9
PubMed 5073686
Publications 1971
[The standpoint of the Committee for Superannuation Benefits]
Tidsskr Nor Laegeforen, 91 (18), 1425-8
PubMed 5568071
Phenotype-genotype correlations in epidermolysis bullosa
Birth Defects Orig Artic Ser, 7 (8), 107-17
PubMed 5173253
Inheritance of Gm(g) and a gene complex Gm a Gm g weak
Clin Genet, 2 (6), 356-66
PubMed 5155313
Publications 1969
Genetics of the Pi serum types. Family studies of the inherited variants of serum alpha-1-antitrypsin
Hum Hered, 19 (4), 354-9
PubMed 5366282
Publications 1968
A note on the PGM-1-PTC linkage relation
Acta Genet Stat Med, 18 (5), 420
PubMed 5755851
Publications 1967
[Single gene diseases: general considerations]
Tidsskr Nor Laegeforen, 87 (5), Suppl:431-8
PubMed 4859969
[Diseases showing an irregular family pattern]
Tidsskr Nor Laegeforen, 87 (5), Suppl:477-83
PubMed 6046761
[Consanguinity and disease]
Tidsskr Nor Laegeforen, 87 (5), Suppl:498-504
PubMed 6046765
[Genetic counseling in hereditary diseases]
Tidsskr Nor Laegeforen, 87 (5), Suppl:507-11
PubMed 6046766
Linkage relations of the phosphoglucomutase PGM locus in man. Probable linkage to phenylthiocarbamid (PTC) taster locus
Acta Genet Stat Med, 17 (6), 482-94
PubMed 6072882
Publications 1966
[Late and early diagnosis of tuberculosis situations]
Tuberkuloza, 18 (1-3), 68-72
PubMed 16296069
Parameters of hemostasis in Epidermolysis bullosa: absence of significant deviations from normal
Acta Derm Venereol, 46 (5), 436-42
PubMed 4162945
Publications 1965
[AAGE JOHANSEN IN MEMORIAM]
Tidsskr Nor Laegeforen, 85, 57
PubMed 14282767
Linkage in man: the Inv and the Lp serum type systems
Nature, 208 (5015), 1126
PubMed 5870581
Publications 1963
[Epidermolysis bullosa congenita simplex with hyperkeratosis palmoplantaris. Therapeutic efforts in a case with generalized blister formation]
Tidsskr Nor Laegeforen, 83, 113-6
PubMed 13946969
[Epidermolysis bullosa hereditaria: orientation and challenge]
Tidsskr Nor Laegeforen, 83, 95-100
PubMed 13946970
Publications 1957
[Consequences of the altered epidemiological situation]
Nord Med, 58 (38), 1421-3
PubMed 13484033
Publications 1956
[Tuberculosis, past, present and future]
Tidsskr Nor Laegeforen, 76 (11), 381-7
PubMed 13337827
Publications 1955
[Gerontology in Norway]
Nord Med, 54 (27), 1051-3
PubMed 13244886
Publications 1952
Tuberculous infection in the light of tuberculin matriculation
Am J Hyg, 56 (2), 139-214
PubMed 12985565
Publications 1951
[Chaos or system in rural health control]
Tidsskr Nor Laegeforen, 71 (17), 550-1
PubMed 14884153
[The duration of BCG allergy]
Nord Med, 45 (4), 122-3
PubMed 14827211
[Declining tuberculosis incidence and control organization]
Nord Med, 46 (31), 1155-8
PubMed 14863714
Publications 1950
[Possibility of determining the effect of mass BCG vaccination]
Nord Med, 43 (10), 444-5
PubMed 14780459
Publications 1949
[Not Available]
Nord Med, 41 (24), 1055-8
PubMed 18135112




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