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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Detalles Bibliográficos
Autores principales: Nouri, Narges, Memarzadeh, Mehrdad, Salehi, Mansoor, Nouri, Nayereh, Meamar, Rokhsareh, Behnam, Mahdiyeh, Derakhshandeh, Fatemeh, Kashkoolinejad, Tahereh, Abdali, Hossein
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2016
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5220684/
https://www.ncbi.nlm.nih.gov/pubmed/28217639
http://dx.doi.org/10.4103/2277-9175.192728

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5220684/
https://www.ncbi.nlm.nih.gov/pubmed/28217639
http://dx.doi.org/10.4103/2277-9175.192728

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