Co-occurrence of chromosome 22q11.2 microdeletion and trisomy 21 mosaicism

American Journal of Medical Genetics

Volumn 112, Issue 1, 2002, Pages 99-102

  Morini, Francesco ^a   Ilari, Michele ^a   Casati, Alessandra ^a   Piserà, Antonietta ^a   Oriolo, Lucia ^a   Cozzi, Denis A ^a  

^a SAPIENZA UNIVERSITY OF ROME   (Italy)

Author keywords

22q11.2; Aberrant right subclavian artery; Down syndrome; Microdeletion; Mosaicism; Pulmonary atresia

Indexed keywords

ANEUPLOIDY; ARTICLE; CHROMOSOMAL LOCALIZATION; CHROMOSOME 21Q; CHROMOSOME 22Q; CHROMOSOME MOSAICISM; CONGENITAL HEART DISEASE; CYTOGENETICS; DISEASE ASSOCIATION; DOWN SYNDROME; FALLOT TETRALOGY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENETIC ASSOCIATION; HEART ATRIUM SEPTUM DEFECT; HUMAN; HUMAN CELL; INFANT; LUNG ATRESIA; PRIORITY JOURNAL; SKIN FIBROBLAST; TRISOMY 21; CASE REPORT; CHROMOSOME 22; MALE; MOSAICISM; NEWBORN;

CASE REPORT; CHROMOSOMES, HUMAN, PAIR 22; DOWN SYNDROME; HUMAN; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT, NEWBORN; MALE; MOSAICISM; HUMANS;

EID: 37649026311     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.10545     Document Type: Article

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