UB Paderborn / Katalog / Suche / in CDI

1 – 18 von 18

Sortiert nach

Age-related macular degeneration and the complement system

Immunobiology (1979), 2012-02, Vol.217 (2), p.127-146

2012

Link zum Volltext

Verfügbarkeit prüfen

Deletions Involving Long-Range Conserved Nongenic Sequences Upstream and Downstream of FOXL2 as a Novel Disease-Causing Mechanism in Blepharophimosis Syndrome

American journal of human genetics, 2005-08, Vol.77 (2), p.205-218

2005

Link zum Volltext

Verfügbarkeit prüfen

EVIDENCE THAT THE GENE FOR TUBEROUS SCLEROSIS IS ON CHROMOSOME 9

The Lancet (British edition), 1987-03, Vol.329 (8534), p.659-661

1987

Link zum Volltext

Verfügbarkeit prüfen

Genetic linkage to the collagen alpha1 (V) gene (COL5A1) in two British Ehlers-Danlos syndrome families with variable type I and II phenotypes

Clinical and experimental dermatology, 1997-07, Vol.22 (4), p.174-176

1997

Link zum Volltext

Verfügbarkeit prüfen

Familial renal cell carcinoma: clinical and molecular genetic aspects

British journal of cancer, 1991-02, Vol.63 (2), p.176-179

1991

Link zum Volltext

Verfügbarkeit prüfen

Mapping of the von Hippel-Lindau disease locus to a small region of chromosome 3p by genetic linkage analysis

Genomics (San Diego, Calif.), 1991, Vol.10 (4), p.957-960

1991

Link zum Volltext

Verfügbarkeit prüfen

Genetic linkage to the collagen α1 (V) gene (COL5A1) in two British Ehlers-Danlos syndrome families with variable type I and II phenotypes

Clinical and experimental dermatology, 1997-07, Vol.22 (4), p.174-176

1997

Link zum Volltext

Verfügbarkeit prüfen

Genetic linkage between Von Hippel—Lindau disease and three microsatellite polymorphisms refines the localisation of the VHL locus

Human molecular genetics, 1993-03, Vol.2 (3), p.279-282

1993

Link zum Volltext

Verfügbarkeit prüfen

Letter to the editor

Genomics (San Diego, Calif.), 1990-07, Vol.7 (3), p.461

1990

Link zum Volltext

Verfügbarkeit prüfen

Physical Mapping within the Tuberous Sclerosis Linkage Group in Region 9q32-q34

Genomics (San Diego, Calif.), 1993-02, Vol.15 (2), p.265-274

1993

Link zum Volltext

Verfügbarkeit prüfen

Genetic Mapping of X-Linked Ocular Albinism: Linkage Analysis in a Large Newfoundland Kindred

Genomics (San Diego, Calif.), 1993-04, Vol.16 (1), p.259-261

1993

Link zum Volltext

Verfügbarkeit prüfen

Deletion of a DNA sequence in eight of nine families with X-linked ichthyosis (steroid sulphatase deficiency)

Nucleic acids research, 1987-05, Vol.15 (10), p.3977-3985

1987

Link zum Volltext

Verfügbarkeit prüfen

Mapping of Von Hippel-Lindau disease to chromosome 3p confirmed by genetic linkage analysis

Journal of the neurological sciences, 1990-12, Vol.100 (1), p.27-30

1990

Link zum Volltext

Verfügbarkeit prüfen

Physical mapping withing the tuberous sclerosis linkage group in region 9q32-q34

Genomics (San Diego, Calif.), 1993-02, Vol.15:2

1993

Link zum Volltext

Verfügbarkeit prüfen

CA repeat polymorphism at the ASS locus

Nucleic acids research, 1990-12, Vol.18 (24), p.7472-7472

1990

Link zum Volltext

Verfügbarkeit prüfen

Physical mapping distal to the DMD locus

Genomics (San Diego, Calif.), 1990-09, Vol.8 (1), p.106-112

1990

Link zum Volltext

Verfügbarkeit prüfen

Tuberous sclerosis: analysis of linkage to red cell and plasma protein markers

Cytogenetics and cell genetics, 1987, Vol.44 (1), p.63

1987

Link zum Volltext

Verfügbarkeit prüfen

Multipoint linkage analysis of steroid sulfatase (X-linked ichthyosis) and distal Xp markers

Genomics (San Diego, Calif.), 1987-09, Vol.1 (1), p.52-59

1987

Link zum Volltext

Verfügbarkeit prüfen

1 – 18 von 18

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(18)
Mit Volltextzugriff
(17)

Publikationsform

Artikel
(18)

Sprache

Englisch
(18)
Japanisch
(2)

Erscheinungsjahr

n.n

Menü

Weitere Dienste

Einstellungen

Age-related macular degeneration and the complement system

Deletions Involving Long-Range Conserved Nongenic Sequences Upstream and Downstream of FOXL2 as a Novel Disease-Causing Mechanism in Blepharophimosis Syndrome

EVIDENCE THAT THE GENE FOR TUBEROUS SCLEROSIS IS ON CHROMOSOME 9

Genetic linkage to the collagen alpha1 (V) gene (COL5A1) in two British Ehlers-Danlos syndrome families with variable type I and II phenotypes

Familial renal cell carcinoma: clinical and molecular genetic aspects

Mapping of the von Hippel-Lindau disease locus to a small region of chromosome 3p by genetic linkage analysis

Genetic linkage to the collagen α1 (V) gene (COL5A1) in two British Ehlers-Danlos syndrome families with variable type I and II phenotypes

Genetic linkage between Von Hippel—Lindau disease and three microsatellite polymorphisms refines the localisation of the VHL locus

Letter to the editor

Physical Mapping within the Tuberous Sclerosis Linkage Group in Region 9q32-q34

Genetic Mapping of X-Linked Ocular Albinism: Linkage Analysis in a Large Newfoundland Kindred

Deletion of a DNA sequence in eight of nine families with X-linked ichthyosis (steroid sulphatase deficiency)

Mapping of Von Hippel-Lindau disease to chromosome 3p confirmed by genetic linkage analysis

Physical mapping withing the tuberous sclerosis linkage group in region 9q32-q34

CA repeat polymorphism at the ASS locus

Physical mapping distal to the DMD locus

Tuberous sclerosis: analysis of linkage to red cell and plasma protein markers

Multipoint linkage analysis of steroid sulfatase (X-linked ichthyosis) and distal Xp markers

Suchergebnisse filtern