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Volumn 22, Issue 3, 2002, Pages 231-234

Can we predict 22q11 status of fetuses with tetralogy of Fallot?

Author keywords

Chromosome 22q; Fetuses; Tetralogy of Fallot

Indexed keywords

ARTICLE; CHROMOSOME 22Q; CONGENITAL HEART MALFORMATION; CONTROLLED STUDY; DISEASE ASSOCIATION; ECHOGRAPHY; FALLOT TETRALOGY; FETUS; FETUS ECHOGRAPHY; GENE DELETION; HUMAN; HYDRAMNIOS; INTRAUTERINE GROWTH RETARDATION; LUNG ATRESIA; MAJOR CLINICAL STUDY; PHENOTYPE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; PULMONARY ARTERY DISEASE;

EID: 0036126081     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/pd.295     Document Type: Article
Times cited : (32)

References (26)
  • 4
    • 0031920989 scopus 로고    scopus 로고
    • Relation of genotype 22q11 deletion to phenotype of pulmonary vessels in tetralogy of Fallot and pulmonary atresia-ventricular septal defect
    • (1998) Heart , vol.79 , pp. 186-190
    • Chessa, M.1    Butera, G.2    Bonhoeffer, P.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.