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A Site-Specific Plectin Mutation Causes Dominant Epidermolysis Bullosa Simplex Ogna: Two Identical De Novo Mutations

Journal of investigative dermatology, 2002-01, Vol.118 (1), p.87-93

2002

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Mutation rate in the hypervariable VNTR g3 (D7S22) is affected by allele length and a flanking DNA sequence polymorphism near the repeat array

American journal of human genetics, 1996-08, Vol.59 (2), p.360-367

1996

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A dedicated internal standard in fragment length analysis of hyperpolymorphic short tandem repeats

Forensic science international, 1997-05, Vol.86 (3), p.207-227

1997

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The human transmembrane secretory component (poly-Ig receptor) : molecular cloning, restriction fragment length polymorphism and chromosomal sublocalization

Human genetics, 1991-10, Vol.87 (6), p.642-648

1991

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Identification by DNA analysis of the victims of the August 1996 Spitsbergen civil aircraft disaster

Nature genetics, 1997-04, Vol.15 (4), p.402-405

1997

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Elevated levels of hypoxanthine in vitreous humor indicate prolonged cerebral hypoxia in victims of sudden infant death syndrome

Pediatrics (Evanston), 1988-10, Vol.82 (4), p.615

1988

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The locus for apolipoprotein E (apoE) is linked to the complement component C3 (C3) locus on chromosome 19 in man

Human genetics, 1982-01, Vol.62 (3), p.233-236

1982

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The gene encoding human transmembrane secretory component (locus PIGR) is linked to D1S58 on chromosome 1

Human genetics, 1992-11, Vol.90 (3), p.215-219

1992

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De Novo Mutations and Allelic Diversity at Minisatellite Locus D7S22 Investigated by Allele-Specific Four-State MVR-PCR Analysis

Human molecular genetics, 1998-12, Vol.7 (13), p.2113-2120

1998

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Distribution of GPT types in Norway

Human heredity, 1975, Vol.25 (1), p.20

Olaisen, B

1975

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The Kidd (JK) blood group locus assigned to chromosome 18 by close linkage to a DNA-RFLP

Human genetics, 1987-11, Vol.77 (3), p.205-209

1987

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DXYS267: DYS393 and its X chromosome counterpart

Forensic science international, 2000-08, Vol.112 (2), p.111-121

2000

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Atypical segregation of erythrocyte glutamic-pyruvic transaminase in a Norwegian family. Evidence of a silent allele

Human heredity, 1973, Vol.23 (6), p.595

Olaisen, B

1973

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C8A and C8B polymorphisms in Norwegians and Norwegian lapps

Human heredity, 1989, Vol.39 (2), p.81

1989

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Fibrinogen gamma chain locus is on chromosome 4 in man

Human genetics, 1982-01, Vol.61 (1), p.24-26

1982

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The C8A and C8B loci are closely linked on chromosome 1

Annals of human genetics, 1986-05, Vol.50 (2), p.139-144

1986

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Studies of HLA, factor B (Bf), complement C2 and C4 haplotypes in type 1 diabetic and control families from northern Sweden

Human heredity, 1986, Vol.36 (4), p.201

1986

Volltextzugriff (PDF)

Genetics of LCAT (lecithin:cholesterol acyltransferase) deficiency

Annals of human genetics, 1975-01, Vol.38 (3), p.327-331

1975

Volltextzugriff (PDF)

Identification of homozygosity for a human apolipoprotein A-I variant

Journal of lipid research, 1986-04, Vol.27 (4), p.436-441

1986

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The ESD polymorphism: further studies of the ESD2 and ESD5 allele products

Human genetics, 1981-01, Vol.57 (4), p.351-353

1981

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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

The Journal of experimental medicine, 1977-11, Vol.146 (5), p.1380-1389

1977

Volltextzugriff (PDF)

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

Human genetics, 1986, Vol.72 (1), p.68-71

1986

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The locus for apolipoprotein E (apoE) is close to the Lutheran (Lu) blood group locus on chromosome 19

Human genetics, 1984-01, Vol.67 (2), p.178-182

1984

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Erythrocyte alanine aminotransferase polymorphism in Norwegian Lapps

Human heredity, 1972, Vol.22 (4), p.380

1972

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Human VNTR mutation and sex

EXS (Basel), 1993, Vol.67, p.63

1993

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A Site-Specific Plectin Mutation Causes Dominant Epidermolysis Bullosa Simplex Ogna: Two Identical De Novo Mutations

Mutation rate in the hypervariable VNTR g3 (D7S22) is affected by allele length and a flanking DNA sequence polymorphism near the repeat array

A dedicated internal standard in fragment length analysis of hyperpolymorphic short tandem repeats

The human transmembrane secretory component (poly-Ig receptor) : molecular cloning, restriction fragment length polymorphism and chromosomal sublocalization

Identification by DNA analysis of the victims of the August 1996 Spitsbergen civil aircraft disaster

Elevated levels of hypoxanthine in vitreous humor indicate prolonged cerebral hypoxia in victims of sudden infant death syndrome

The locus for apolipoprotein E (apoE) is linked to the complement component C3 (C3) locus on chromosome 19 in man

The gene encoding human transmembrane secretory component (locus PIGR) is linked to D1S58 on chromosome 1

De Novo Mutations and Allelic Diversity at Minisatellite Locus D7S22 Investigated by Allele-Specific Four-State MVR-PCR Analysis

Distribution of GPT types in Norway

The Kidd (JK) blood group locus assigned to chromosome 18 by close linkage to a DNA-RFLP

DXYS267: DYS393 and its X chromosome counterpart

Atypical segregation of erythrocyte glutamic-pyruvic transaminase in a Norwegian family. Evidence of a silent allele

C8A and C8B polymorphisms in Norwegians and Norwegian lapps

Fibrinogen gamma chain locus is on chromosome 4 in man

The C8A and C8B loci are closely linked on chromosome 1

Studies of HLA, factor B (Bf), complement C2 and C4 haplotypes in type 1 diabetic and control families from northern Sweden

Genetics of LCAT (lecithin:cholesterol acyltransferase) deficiency

Identification of homozygosity for a human apolipoprotein A-I variant

The ESD polymorphism: further studies of the ESD2 and ESD5 allele products

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

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

The locus for apolipoprotein E (apoE) is close to the Lutheran (Lu) blood group locus on chromosome 19

Erythrocyte alanine aminotransferase polymorphism in Norwegian Lapps

Human VNTR mutation and sex

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