COL5a1: fine genetic mapping and exclusion as candidate gene in families with nail-patella syndrome, tuberous sclerosis 1, hereditary hemorrhagic telangiectasia, and Ehlers—Danlos syndrome type II
Open Access
- 10 February 1995
- Vol. 25 (3) , 737-739
- https://doi.org/10.1016/0888-7543(95)80021-d
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- REPORT on the Third International Workshop on Chromosome 9Annals of Human Genetics, 1994
- BstUI and Dpnll RFLPs at the COL5A1 geneHuman Molecular Genetics, 1994
- A disease locus for hereditary haemorrhagic telangiectasia maps to chromosome 9q33–34Nature Genetics, 1994
- Deletion of the Paired α5(IV) and α6(IV) Collagen Genes in Inherited Smooth Muscle TumorsScience, 1993
- Type V collagen: molecular structure and fibrillar organization of the chicken alpha 1(V) NH2-terminal domain, a putative regulator of corneal fibrillogenesis.The Journal of cell biology, 1993
- Human collagen gene COL5A1 maps to the q34.2→q34.3 region of chromosome 9, near the locus for nail-patella syndromeGenomics, 1992
- SEGREGATION ANALYSIS OF THE STRUCTURAL GENES OF THE MAJOR FIBRILLAR COLLAGENS PROVIDES FURTHER EVIDENCE OF MOLECULAR HETEROGENEITY IN TYPE II EHLERS—DANLOS SYNDROMERheumatology, 1991
- Familial Ehlers‐Danlos Syndrome Type II: Abnormal Fibrillogenesis of Dermal CollagenPediatric Dermatology, 1987
- MAPMAKER: An interactive computer package for constructing primary genetic linkage maps of experimental and natural populationsGenomics, 1987