Linkage analysis in dominantly inherited osteogenesis imperfecta-Reference-Cited by-同舟云学术

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Linkage analysis in dominantly inherited osteogenesis imperfecta

Published:1993-01-15 Issue:2 Volume:45 Page:212-216
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Sykes Bryan

Publisher

Wiley

Subject

Genetics(clinical)

Reference11 articles.

1. 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.

2. Location on Chromosome 15 of the Gene Defect Causing Marfan Syndrome

3. et al. (1992) Prenatal diagnosis of osteogenesis imperfecta by identification of the concordant collagen 1 allele. J Med Genet (in press).

4. Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene

5. Segregation analysis of dominant osteogenesis imperfecta in Italy.

Cited by 18 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. Mutational Screening of Skeletal Genes in 14 Chinese Children with Osteogenesis Imperfecta Using Targeted Sequencing;Journal of Immunology Research;2022-05-19

2. Tooth agenesis in osteogenesis imperfecta related to mutations in the collagen type I genes;Oral Diseases;2016-09-13

3. A novel frameshift deletion in the COL1A1 gene identified in a Chinese family with osteogenesis imperfecta;Genetics and Molecular Research;2015

4. Mutation characteristics in type I collagen genes in Chinese patients with osteogenesis imperfecta;Genetics and Molecular Research;2011

5. Bone mineral content and collagen defects in osteogenesis imperfecta;Acta Paediatrica;2007-01-02

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