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Karyotype 45,XX,−21/46,XX,21q− in an infant with symptoms of G-deletion syndrome I

An infant with antimongoloid eye slants, achalasia, broad nose, one low-set large and one rudimentary ear lobe, and rudimentary nails with a retarded psychomotor development showed an 45,XX,−21/46,XX,21q− karyotype. By fluorescence and Giemsa staining it was shown that the missing or deleted chromos...

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Detaylı Bibliyografya
Yayımlandı:J Med Genet
Asıl Yazarlar: Mikkelsen, Margareta, Vestermark, S.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BMJ Publishing Group 1974
Konular:
Online Erişim:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC1013215/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/4140913/
https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jmg.11.4.389
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