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Volumn 17, Issue 1, 2002, Pages 125-128

Prenatal diagnosis of tetralogy of Fallot associated with chromosome 22q11 deletion.

Author keywords

[No Author keywords available]

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;

EID: 0036480714     PISSN: 10118934     EISSN: None     Source Type: Journal    
DOI: 10.3346/jkms.2002.17.1.125     Document Type: Article
Times cited : (11)

References (0)
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.