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An interstitial deletion of chromosome 9 in a girl with multiple congenital anomalies.

An infant with peculiar facies, coloboma of both eyes, and developmental retardation was found to have d de novo interstitial deletion of the secondary constriction and some adjacent euchromatin on one of her No. 9 chromosomes, del(9)(q11q21). Since studies on duplications, variants, and the molecul...

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Detaylı Bibliyografya
Asıl Yazarlar: Wisniewski, L, Purdy, G, Hassold, T, Wilson, C, Bentley, K, Hackel, E, Higgins, J V
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 1977
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC1013645/
https://ncbi.nlm.nih.gov/pubmed/604498
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