Interstitial deletion of 10p and atrial septal defect in DiGeorge 2 syndrome

Clinical Genetics

Volumn 66, Issue 2, 2004, Pages 128-136

  Yatsenko, S A ^a   Yatsenko, A N ^a   Szigeti, K ^a   Craigen, W J ^a   Stankiewicz, P ^a   Cheung, S W ^a   Lupski, James R ^a,b  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

^b TEXAS CHILDREN S HOSPITAL   (United States)

Author keywords

Atrial septal defect; Critical region; Deletion 10p; DiGeorge 2 syndrome; NEBL

Indexed keywords

TRANSCRIPTION FACTOR;

ARTICLE; CHILD; CHROMOSOME 10P; CHROMOSOME DELETION; CHROMOSOME HIGH RESOLUTION BANDING ANALYSIS; CONGENITAL HEART MALFORMATION; CONGENITAL MALFORMATION; DEVELOPMENTAL DISORDER; DIGEORGE SYNDROME; DISEASE ASSOCIATION; EBSTEIN ANOMALY; ECHOCARDIOGRAPHY; FACE DYSMORPHIA; FLUORESCENCE IN SITU HYBRIDIZATION; FREQUENCY ANALYSIS; GENE DELETION; GENETIC ANALYSIS; GENOTYPE PHENOTYPE CORRELATION; HEART ATRIUM SEPTUM DEFECT; HUMAN; KIDNEY MALFORMATION; MALE; MITRAL VALVE REGURGITATION; MOLECULAR CLONING; MOLECULAR GENETICS; PRIORITY JOURNAL; TRICUSPID VALVE REGURGITATION;

CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 10; CYTOGENETIC ANALYSIS; DIGEORGE SYNDROME; ECHOCARDIOGRAPHY; FEMALE; HEART DEFECTS, CONGENITAL; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; KLEBSIELLA INFECTIONS; MALE;

EID: 4344669334     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1399-0004.2004.00290.x     Document Type: Article

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