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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Dades bibliogràfiques
Publicat a:Adv Biomed Res
Autors principals: Nouri, Narges, Memarzadeh, Mehrdad, Salehi, Mansoor, Nouri, Nayereh, Meamar, Rokhsareh, Behnam, Mahdiyeh, Derakhshandeh, Fatemeh, Kashkoolinejad, Tahereh, Abdali, Hossein
Format: Artigo
Idioma:Inglês
Publicat: Medknow Publications & Media Pvt Ltd 2016
Matèries:
Original Article
Accés en línia: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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