Detection of a high frequency RsaI polymorphism in the human pro alpha 2(I) collagen gene which is linked to an autosomal dominant form of osteogenesis imperfecta.-Reference-Cited by-同舟云学术

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Detection of a high frequency RsaI polymorphism in the human pro alpha 2(I) collagen gene which is linked to an autosomal dominant form of osteogenesis imperfecta.

Published:1985-07 Issue:7 Volume:4 Page:1745-1748
ISSN:0261-4189
Container-title:The EMBO Journal
language:en
Short-container-title:The EMBO Journal

Author:

Grobler-Rabie A.F.,Wallis G.,Brebner D.K.,Beighton P.,Bester A.J.,Mathew C.G.

Publisher

Wiley

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,Molecular Biology,General Neuroscience

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/j.1460-2075.1985.tb03845.x/fullpdf

Cited by 45 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. COL1A2 gene deletion polymorphism in an Italian and an Ivorian populations;Russian Journal of Genetics;2009-07

2. Petros Tsipouras4;Clinical Genetics;2008-04-23

3. Deletions and duplications of Gly-Xaa-Yaa triplet repeats in the triple helical domains of type I collagen chains disrupt helix formation and result in several types of osteogenesis imperfecta;Human Mutation;2001

4. Osteogenesis Imperfecta;Metabolic Bone Disease and Clinically Related Disorders;1998

5. A Gly859Ser substitution in the triple helical domain of the α2 chain of type I collagen resulting in osteogenesis imperfecta type III in two unrelated individuals;Human Mutation;1994

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