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

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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Bibliographic Details
Main Authors: Narges Nouri, Mehrdad Memarzadeh, Mansoor Salehi, Nayereh Nouri, Rokhsareh Meamar, Mahdiyeh Behnam, Fatemeh Derakhshandeh, Tahereh Kashkoolinejad, Hossein Abdali
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2016-01-01
Series:Advanced Biomedical Research
Subjects:
Chromosome 22q11.2 deletion syndrome
cleft palate
developmental delay
DiGeorge syndrome
Iranian
Online Access:http://www.advbiores.net/article.asp?issn=2277-9175;year=2016;volume=5;issue=1;spage=201;epage=201;aulast=Nouri

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http://www.advbiores.net/article.asp?issn=2277-9175;year=2016;volume=5;issue=1;spage=201;epage=201;aulast=Nouri

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