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Volumn 21, Issue 2, 2005, Pages

Obstetrics

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ALAGILLE SYNDROME; AMNIOCENTESIS; ARTICLE; AUTOPSY; CASE REPORT; CATCH 22 SYNDROME; CHROMOSOME 22Q; CHROMOSOME DELETION; CLEFT PALATE; CLINICAL FEATURE; CLUBFOOT; CONGENITAL HEART MALFORMATION; CONGENITAL MALFORMATION; DEVELOPMENTAL DISORDER; DIFFERENTIAL DIAGNOSIS; DIGEORGE SYNDROME; FACE DYSMORPHIA; FALLOT TETRALOGY; FAMILY HISTORY; FEMALE; FETUS ECHOGRAPHY; FLUORESCENCE IN SITU HYBRIDIZATION; GOLDENHAR SYNDROME; HEART VENTRICLE SEPTUM DEFECT; HETEROZYGOTE; HUMAN; HYPOPLASIA; HYPOPLASTIC LEFT HEART SYNDROME; INCIDENCE; KIDNEY MALFORMATION; MENTAL DISEASE; NEWBORN; NEWBORN DEATH; PALATOPHARYNGEAL INCOMPETENCE; PATENT DUCTUS ARTERIOSUS; POLYDACTYLY; PRIORITY JOURNAL; RECURRENCE RISK; SHORT STATURE; SMITH LEMLI OPITZ SYNDROME; SYNDACTYLY; SYNDROME VACTERL; THYMUS DISEASE; THYMUS HYPOPLASIA; VELOCARDIOFACIAL SYNDROME; VERTEBRA MALFORMATION; ECHOGRAPHY; PREGNANCY;

EID: 19544373429     PISSN: 08948771     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (3)

References (4)
  • 4
    • 19544367552 scopus 로고    scopus 로고
    • Prenatal diagnosis of 22q11 deletion: A series of 5 cases with congenital heart defects
    • Raymond FL, et al. Prenatal diagnosis of 22q11 deletion: a series of 5 cases with congenital heart defects. J Med Genet. 1997;17:263-267.
    • (1997) J Med Genet , vol.17 , pp. 263-267
    • Raymond, F.L.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.