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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Detalhes bibliográficos
Publicado no:Adv Biomed Res
Main Authors: Nouri, Narges, Memarzadeh, Mehrdad, Salehi, Mansoor, Nouri, Nayereh, Meamar, Rokhsareh, Behnam, Mahdiyeh, Derakhshandeh, Fatemeh, Kashkoolinejad, Tahereh, Abdali, Hossein
Formato: Artigo
Idioma:Inglês
Publicado em: Medknow Publications & Media Pvt Ltd 2016
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Original Article
Acesso em linha: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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