22q11 microdeletion studies in the heart tissue of an abortus involving a familial form of congenital heart disease

Journal of Clinical Laboratory Analysis

Volumn 20, Issue 4, 2006, Pages 160-163

  Patel, Zareen M ^a,b   Gawde, H M ^a   Khatkhatay, M I ^a  

^a NATIONAL INSTITUTE FOR RESEARCH IN REPRODUCTIVE HEALTH   (India)

^b INDIAN COUNCIL OF MEDICAL RESEARCH   (India)

Author keywords

CHD; Chromosome 22q11.2; Familial; FISH

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CELL LINE; CHROMOSOME 22Q; CHROMOSOME DELETION; CHROMOSOME MOSAICISM; CONGENITAL HEART DISEASE; DIAGNOSTIC VALUE; DIGEORGE SYNDROME; ECHOGRAPHY; FAMILY HISTORY; FEMALE; FETUS; FLUORESCENCE IN SITU HYBRIDIZATION; HEART; HUMAN; HUMAN CELL; HUMAN TISSUE; PERIPHERAL LYMPHOCYTE; PRENATAL DIAGNOSIS; SPONTANEOUS ABORTION; VELOCARDIOFACIAL SYNDROME;

ABORTED FETUS; ADULT; CELL NUCLEUS; CHROMOSOME BANDING; CHROMOSOMES, HUMAN, PAIR 22; FAMILY HEALTH; FEMALE; GENE DELETION; HEART; HEART DEFECTS, CONGENITAL; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MYOCARDIUM; PREGNANCY;

EID: 33746905482     PISSN: 08878013     EISSN: 10982825     Source Type: Journal    
DOI: 10.1002/jcla.20125     Document Type: Article

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