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Volumn 17, Issue 1, 2002, Pages 125-128
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Prenatal diagnosis of tetralogy of Fallot associated with chromosome 22q11 deletion.
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Author keywords
[No Author keywords available]
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Indexed keywords
ADULT;
ARTICLE;
CASE REPORT;
CHROMOSOME 22;
CHROMOSOME DELETION;
ECHOCARDIOGRAPHY;
FALLOT TETRALOGY;
FEMALE;
FETUS DISEASE;
FLUORESCENCE IN SITU HYBRIDIZATION;
GENETICS;
HUMAN;
METHODOLOGY;
PREGNANCY;
PRENATAL DIAGNOSIS;
ADULT;
CHROMOSOME DELETION;
CHROMOSOMES, HUMAN, PAIR 22;
ECHOCARDIOGRAPHY;
FEMALE;
FETAL DISEASES;
HUMANS;
IN SITU HYBRIDIZATION, FLUORESCENCE;
PREGNANCY;
PRENATAL DIAGNOSIS;
TETRALOGY OF FALLOT;
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EID: 0036480714
PISSN: 10118934
EISSN: None
Source Type: Journal
DOI: 10.3346/jkms.2002.17.1.125 Document Type: Article |
Times cited : (11)
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References (0)
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