Recurrence of fibrochondrogenesis in a consanguineous family-Reference-Cited by-同舟云学术

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Recurrence of fibrochondrogenesis in a consanguineous family

Published:1999-01 Issue:1 Volume:8 Page:59???62
ISSN:0962-8827
Container-title:Clinical Dysmorphology
language:en
Short-container-title:Clinical Dysmorphology

Author:

Al-Gazali L. I.,Bakir M.,Dawodu A.,Haas D.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Genetics (clinical),General Medicine,Pathology and Forensic Medicine,Anatomy,Pediatrics, Perinatology and Child Health

Cited by 5 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. Dominant and recessive forms of fibrochondrogenesis resulting from mutations at a second locus, COL11A2;American Journal of Medical Genetics Part A;2012-01-13

2. Clinical and molecular analysis of UAE fibrochondrogenesis patients expands the phenotype and reveals two COL11A1 homozygous null mutations;Clinical Genetics;2011-07-18

3. Fibrochondrogenesis Results from Mutations in the COL11A1 Type XI Collagen Gene;The American Journal of Human Genetics;2010-11

4. THE FETAL MUSCULOSKELETAL SYSTEM;Ultrasonography in Obstetrics and Gynecology;2008

5. F;Taybi and Lachman's Radiology of Syndromes, Metabolic Disorders and Skeletal Dysplasias;2007

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