Microsatellite DNA markers detects 95% of chromosome 22q11 deletions

American Journal of Medical Genetics

Volumn 68, Issue 2, 1997, Pages 182-184

  Bonnet, Damien ^a   Cormier Daire, Valérie ^a   Kachaner, Jean ^a   Szezepanski, Isabelle ^a   Souillard, Patrick ^a   Sidi, Daniel ^a   Munnich, Arnold ^a   Lyonnet, Stanislas ^a  

^a HÔPITAL NECKER ENFANTS MALADES   (France)

Author keywords

chromosome 22q11.2 microdeletions; congenital heart disease; conotruncal heart defect; microsatellite DNA markers

Indexed keywords

DNA MARKER; MICROSATELLITE DNA;

ARTICLE; CHROMOSOME 22Q; CHROMOSOME DELETION; CLINICAL ARTICLE; CONGENITAL HEART MALFORMATION; DIGEORGE SYNDROME; HUMAN; INHERITANCE; MALFORMATION SYNDROME; NEWBORN; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL;

ALLELES; CHROMOSOMES, HUMAN, PAIR 22; DIGEORGE SYNDROME; HEART DEFECTS, CONGENITAL; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT, NEWBORN; MICROSATELLITE REPEATS; PEDIGREE; POLYMERASE CHAIN REACTION; SEQUENCE DELETION;

EID: 0031052948     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19970120)68:2<182::AID-AJMG12>3.0.CO;2-Q     Document Type: Article

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