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1p36 deletion syndrome: an update

Deletions of chromosome 1p36 affect approximately 1 in 5,000 newborns and are the most common terminal deletions in humans. Medical problems commonly caused by terminal deletions of 1p36 include developmental delay, intellectual disability, seizures, vision problems, hearing loss, short stature, dis...

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Detaylı Bibliyografya
Yayımlandı:Appl Clin Genet
Asıl Yazarlar: Jordan, Valerie K, Zaveri, Hitisha P, Scott, Daryl A
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Dove Medical Press 2015
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4555966/
https://ncbi.nlm.nih.gov/pubmed/26345236
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/TACG.S65698
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