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Volumn 39, Issue 4, 2002, Pages
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Chromosome 10p13-14 and 22q11 deletion screening in 100 patients with isolated and syndromic conotruncal heart defects.
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NONE
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Author keywords
[No Author keywords available]
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Indexed keywords
ADULT;
CHILD;
CHROMOSOME 10;
CHROMOSOME 22;
CHROMOSOME DELETION;
CONGENITAL HEART MALFORMATION;
GENETIC SCREENING;
GENETICS;
HUMAN;
INFANT;
LETTER;
MIDDLE AGED;
NEWBORN;
PRESCHOOL CHILD;
PROSPECTIVE STUDY;
SYNDROME;
ADULT;
CHILD;
CHILD, PRESCHOOL;
CHROMOSOME DELETION;
CHROMOSOMES, HUMAN, PAIR 10;
CHROMOSOMES, HUMAN, PAIR 22;
GENETIC SCREENING;
HEART DEFECTS, CONGENITAL;
HUMANS;
INFANT;
INFANT, NEWBORN;
MIDDLE AGED;
PROSPECTIVE STUDIES;
SYNDROME;
MLCS;
MLOWN;
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EID: 0036548382
PISSN: None
EISSN: 14686244
Source Type: Journal
DOI: 10.1136/jmg.39.4.e16 Document Type: Letter |
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Times cited : (13)
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References (0)
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