Prevalence of 22q11.2 microdeletion in 146 patients with cardiac malformation in a referral hospital of North India

BMC Medical Genetics

Volumn 11, Issue 1, 2010, Pages

  Halder, Ashutosh ^a   Jain, Manish ^a   Chaudhary, Isha ^a   Kabra, Madhulika ^a  

^a ALL INDIA INSTITUTE OF MEDICAL SCIENCES   (India)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CHILD; CHROMOSOME 21Q; CHROMOSOME DELETION; CLINICAL ARTICLE; CLINICAL FEATURE; CONGENITAL HEART MALFORMATION; CONTROLLED STUDY; FACE DYSMORPHIA; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENETIC ASSOCIATION; GENETIC SCREENING; HUMAN; HYPOCALCEMIA; INDIA; INFANT; MALE; MICRODELETION SYNDROME; PATIENT REFERRAL; PRESCHOOL CHILD; SCHOOL CHILD; CHROMOSOME 22; GENETICS; KARYOTYPING; PREVALENCE;

CHILD; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; FEMALE; HEART DEFECTS, CONGENITAL; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INDIA; INFANT; KARYOTYPING; MALE; PREVALENCE;

EID: 77953719529     PISSN: None     EISSN: 14712350     Source Type: Journal    
DOI: 10.1186/1471-2350-11-101     Document Type: Article

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