A gene for cleidocranial dysplasia maps to the short arm of chromosome 6.

Cleidocranial dysplasia (CCD) is an autosomal dominant generalized bone dysplasia characterized by mild-to-moderate short stature, clavicular aplasia or hypoplasia, supernumerary and ectopic teeth, delayed eruption of secondary teeth, a characteristic craniofacial appearance, and a variety of other...

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Hlavní autoři: Feldman, G J, Robin, N H, Brueton, L A, Robertson, E, Thompson, E M, Siegel-Bartelt, J, Gasser, D L, Bailey, L C, Zackai, E H, Muenke, M
Médium: Artigo
Jazyk:Inglês
Vydáno: 1995
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Research Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1801197/
https://ncbi.nlm.nih.gov/pubmed/7717404
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