Terminal deletion (14)(q32.3): a new case.

A mildly dysmorphic, 2 year old girl with mental retardation was found to have a small de novo terminal deletion of the long arm of chromosome 14, del(14)(q32.3). She was found to have features in common with two previous terminal deletion cases and particularly with the well documented ring 14 synd...

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Detaylı Bibliyografya
Yayımlandı:J Med Genet
Asıl Yazarlar: Telford, N, Thomson, D A, Griffiths, M J, Ilett, S, Watt, J L
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BMJ Publishing Group 1990
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC1017031/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2182875/
https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jmg.27.4.261
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