Linkage Studies of a Missouri Kindred with Autosomal Dominant Spondyloepimetaphyseal Dysplasia (SEMD) Indicate Genetic Heterogeneity-Reference-Cited by-同舟云学术

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Linkage Studies of a Missouri Kindred with Autosomal Dominant Spondyloepimetaphyseal Dysplasia (SEMD) Indicate Genetic Heterogeneity

Published:1997-08-01 Issue:8 Volume:12 Page:1204-1209
ISSN:0884-0431
Container-title:Journal of Bone and Mineral Research
language:en
Short-container-title:J Bone Miner Res

Author:

Gertner Joseph M.,Whyte Michael P.,Dixon Peter H.,Pang Joanna T.,Trump Dorothy,Pearce Simon H. S.,Wooding Carol,Thakker Rajesh V.

Publisher

Wiley

Subject

Orthopedics and Sports Medicine,Endocrinology, Diabetes and Metabolism

Reference45 articles.

1. Spondylometepiphyseal dysplasia congenita, Strudwick Type;Shebib;Pediatr Radiol,1991

Cited by 11 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. A de novo variant in MMP13 identified in a patient with dominant metaphyseal anadysplasia;European Journal of Medical Genetics;2019-11

2. Matrix metalloproteinases and bone;Bone;2008-07

3. MMP13 mutation causes spondyloepimetaphyseal dysplasia, Missouri type (SEMDMO);Journal of Clinical Investigation;2005-10-01

4. Altered endochondral bone development in matrix metalloproteinase 13-deficient mice;Development;2004-12-01

5. Lexikalischer Teil;Lexikon der Syndrome und Fehlbildungen;2003

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