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Volumn 118 A, Issue 4, 2003, Pages 319-327

Prenatal detection of rare chromosomal autosomal abnormalities in Europe

(31)  Baena, Neus a,g   De Vigan, C b   Cariati, E c   Clementi, M d   Stoll, C e   Caballin, M R f   Guitart, M a   Haeusler, M h   Barisic, I h   Matejic, R h   Garne, E h   Vodovar, V h   Alembik, Y h   Dott, B h   Froster, U G h   Queisser Luft, A h   Wiesel, A h   Tenconi, R h   Benedicenti, F h   Bianca, S h   more..

b INSERM   (France)
h NONE

Author keywords

Congenital anomaly; Congenital malformation; Prenatal diagnosis; Rare chromosomal autosomal abnormalities; Ultrasound

Indexed keywords

ADULT; ARTICLE; AUTOSOMAL DISORDER; CENTRAL NERVOUS SYSTEM MALFORMATION; CHROMOSOME ABERRATION; CHROMOSOME DELETION; CHROMOSOME DUPLICATION; CHROMOSOME REARRANGEMENT; CONGENITAL HEART MALFORMATION; CONGENITAL MALFORMATION; CYSTIC LYMPHANGIOMA; DIAPHRAGM DISEASE; EUROPE; FEMALE; FETUS; HUMAN; MAJOR CLINICAL STUDY; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; TRISOMY; ULTRASOUND;

EID: 0042832501     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.a.10104     Document Type: Article
Times cited : (16)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.