Genetic heterogeneity of Saethre-Chotzen syndrome, due to TWIST and FGFR mutations.

Thirty-two unrelated patients with features of Saethre-Chotzen syndrome, a common autosomal dominant condition of craniosynostosis and limb anomalies, were screened for mutations in TWIST, FGFR2, and FGFR3. Nine novel and three recurrent TWIST mutations were found in 12 families. Seven families were...

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Detaylı Bibliyografya
Asıl Yazarlar: Paznekas, W A, Cunningham, M L, Howard, T D, Korf, B R, Lipson, M H, Grix, A W, Feingold, M, Goldberg, R, Borochowitz, Z, Aleck, K, Mulliken, J, Yin, M, Jabs, E W
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 1998
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC1377134/
https://ncbi.nlm.nih.gov/pubmed/9585583
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