Investigation of TBX1 gene deletion in Iranian children with 22q11.2 deletion syndrome: correlation with conotruncal heart defects

BACKGROUND: DiGeorge syndrome (DGS) is the result of a microdeletion in chromosome 22q11.2 in over 90% of cases. DGS is the second most frequent syndrome after Down syndrome and has an incidence of 1/4000 births. Unequal crossover between low-copy repeats, on the proximal part of the long arm of chr...

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Detalhes bibliográficos
Publicado no:Heart Asia
Main Authors: Ganji, Hamid, Salehi, Mansoor, Sedghi, Maryam, Abdali, Hossein, Nouri, Nayereh, Sadri, Leyli, Hosseinzadeh, Majid, Vakili, Bahareh, Lotfi, Mahdi
Formato: Artigo
Idioma:Inglês
Publicado em: BMJ Publishing Group 2013
Assuntos:
Original Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4832817/
https://ncbi.nlm.nih.gov/pubmed/27326128
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/heartasia-2013-010327
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