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

✍ Scribed by Ganji, H.; Salehi, M.; Sedghi, M.; Abdali, H.; Nouri, N.; Sadri, L.; Hosseinzadeh, M.; Vakili, B.; Lotfi, M.

Book ID: 127249379
Publisher: BMJ
Year: 2013
Tongue: English
Weight: 83 KB
Volume: 5
Category: Article
ISSN: 1759-1104
DOI: 10.1136/heartasia-2013-010327

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