Prevalence of 22q11.2 microdeletion syndrome in Iranian patients with cleft palate

BACKGROUND: 22q11.2 microdeletion syndrome is the most common multiple genetic disorder associated with learning disabilities, developmental delays, immune deficiency, hypocalcemia, and cleft palate. Finding some valid criteria for screening of 22q11.2 deletion syndromes in infants would be very hel...

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Bibliografiska uppgifter
I publikationen:Adv Biomed Res
Huvudupphovsmän: Nouri, Narges, Memarzadeh, Mehrdad, Salehi, Mansoor, Nouri, Nayereh, Meamar, Rokhsareh, Behnam, Mahdiyeh, Derakhshandeh, Fatemeh, Kashkoolinejad, Tahereh, Abdali, Hossein
Materialtyp: Artigo
Språk:Inglês
Publicerad: Medknow Publications & Media Pvt Ltd 2016
Ämnen:
Original Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC5220684/
https://ncbi.nlm.nih.gov/pubmed/28217639
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/2277-9175.192728
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