Heterotrisomy, a significant contributing factor to ventricular septal defect associated with Down syndrome?

Human Genetics

Volumn 107, Issue 5, 2000, Pages 476-482

  Baptista, M J ^a   Fairbrother, U L ^a   Howard, C M ^a   Farrer, M J ^a   Davies, G E ^a   Trikka, D ^a   Maratou, K ^a   Redington, A ^a   Greve, G ^a   Njolstad, P R ^a   Kessling, A M ^a  

^a IMPERIAL COLLEGE LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; ARTICLE; CHILD; CHROMOSOME 21; CLINICAL FEATURE; DISEASE ASSOCIATION; DOWN SYNDROME; FEMALE; GENETIC ANALYSIS; GENETIC MARKER; GENETIC POLYMORPHISM; GENETIC PREDISPOSITION; HEART VENTRICLE SEPTUM DEFECT; HETEROZYGOSITY; HUMAN; INHERITANCE; MAJOR CLINICAL STUDY; MALE; PARENT; PRIORITY JOURNAL; RISK FACTOR; TRISOMY 21;

ADULT; CHILD; CHROMOSOMES, HUMAN, PAIR 21; DOWN SYNDROME; FEMALE; GENETIC MARKERS; GENOMIC IMPRINTING; HEART DEFECTS, CONGENITAL; HEART SEPTAL DEFECTS, VENTRICULAR; HETEROZYGOTE DETECTION; HUMANS; MALE; NUCLEAR FAMILY; POLYMORPHISM, GENETIC; TRISOMY;

EID: 17744384959     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390000395     Document Type: Article

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