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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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Pubblicato in:Appl Clin Genet
Autori principali: Jordan, Valerie K, Zaveri, Hitisha P, Scott, Daryl A
Natura: Artigo
Lingua:Inglês
Pubblicazione: Dove Medical Press 2015
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Accesso online: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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