The gene for Treacher Collins syndrome maps to the long arm of chromosome 5.

Treacher Collins syndrome (TCS) is an autosomal dominant disorder of craniofacial development, the features of which include conductive hearing loss and cleft palate. We have studied 12 unrelated TCS families with multiple affected individuals for linkage to five chromosome 5 markers. There is stron...

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Detaylı Bibliyografya
Asıl Yazarlar: Dixon, M J, Read, A P, Donnai, D, Colley, A, Dixon, J, Williamson, R
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 1991
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC1683211/
https://ncbi.nlm.nih.gov/pubmed/1676560
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