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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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Bibliografiske detaljer
Udgivet i:Appl Clin Genet
Main Authors: Jordan, Valerie K, Zaveri, Hitisha P, Scott, Daryl A
Format: Artigo
Sprog:Inglês
Udgivet: Dove Medical Press 2015
Fag:
Online adgang: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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