Microdeletion study in children with selective congenital heart disease; an Iranian multicenter study

Ali Akbar, Zeinaloo; Abdorazaagh, Kiani; Parvin, Akbari Asbagh; M. R., Noori Dalooi; Elham, Ghadami Yazdi; Tayebeh, Sabokbar; Asgar, Aghamohammadi; Mahmood Gholam, Ale Mohammad; Sima, Rafeyan; Jila, Dastan; Saeed Reza, Ghaffari

Ali Akbar, Zeinaloo; Abdorazaagh, Kiani; Parvin, Akbari Asbagh; M. R., Noori Dalooi; Elham, Ghadami Yazdi; Tayebeh, Sabokbar; Asgar, Aghamohammadi; Mahmood Gholam, Ale Mohammad; Sima, Rafeyan; Jila, Dastan; Saeed Reza, Ghaffari.

Iranian Journal of Pediatrics. 2009; 19 (1): 11-17

in En | IMEMR | ID: emr-91412

Responsible library: EMRO

Subject(s)

Humans; Male; Female; Heart Defects, Congenital/etiology; In Situ Hybridization, Fluorescence/statistics & numerical data; DiGeorge Syndrome/congenital; DiGeorge Syndrome/genetics; /etiology; /genetics; Pulmonary Atresia/etiology; Pulmonary Atresia/genetics; Chromosome Deletion; Pulmonary Subvalvular Stenosis/etiology; Pulmonary Subvalvular Stenosis/genetics; Prenatal Diagnosis/standards; Truncus Arteriosus; Heart Septal Defects, Ventricular/etiology; Heart Septal Defects, Ventricular/genetics

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Index: IMEMR Main subject: Prenatal Diagnosis / Pulmonary Subvalvular Stenosis / Truncus Arteriosus / Chromosome Deletion / In Situ Hybridization, Fluorescence / Pulmonary Atresia / DiGeorge Syndrome / Heart Defects, Congenital / Heart Septal Defects, Ventricular Type of study: Clinical_trials Limits: Female / Humans / Male Language: En Journal: Iran. J. Pediatr. Year: 2009

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