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Volumn 27, Issue 6, 1998, Pages 625-628

Congenital heart disease and nuchal translucency with normal caryotype, report of three cases;Cardiopathie congenitale et clarte nucale avec caryotype normal: A propos de 3 cas

Author keywords

Congenital heart disease; Nuchal translucency; Ultrasound; Williams Beuren syndrome

Indexed keywords

ADULT; ARTICLE; CLINICAL ARTICLE; CONGENITAL HEART DISEASE; FEMALE; FETUS; FETUS ECHOGRAPHY; FIRST TRIMESTER PREGNANCY; HUMAN; HYPOPLASTIC LEFT HEART SYNDROME; PULMONARY VALVE STENOSIS; TRANSVAGINAL ECHOGRAPHY; WILLIAMS BEUREN SYNDROME; CARDIOMEGALY; CASE REPORT; ECHOGRAPHY; GENETICS; KARYOTYPING; MUTATION; NECK; PREGNANCY; PRENATAL DEVELOPMENT;

EID: 0031732885     PISSN: 03682315     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (2)

References (11)
  • 1
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  • 3
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    • Hyett J, Moscoso G, Papapanagiotou G, Perdu M, Nicolaides KH. Abnormalities of the heart and great arteries in chromosomally normal fetuses with increased nuchal tanslucency thickness at 11-13 weeks of gestation. Ultrasound Obstet Gynecol 1996;7:245-50.
    • (1996) Ultrasound Obstet Gynecol , vol.7 , pp. 245-250
    • Hyett, J.1    Moscoso, G.2    Papapanagiotou, G.3    Perdu, M.4    Nicolaides, K.H.5
  • 4
    • 0030724595 scopus 로고    scopus 로고
    • Increased nuchal translucency at 10-14 weeks of gestation as a marker for major cardiac defects
    • Hyett J, Perdu M, Sharland G, Snijders R, Nicolaides KH. Increased nuchal translucency at 10-14 weeks of gestation as a marker for major cardiac defects. Ultrasound Obstet Gynecol 1997;10:242-6.
    • (1997) Ultrasound Obstet Gynecol , vol.10 , pp. 242-246
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  • 5
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    • Online Mendelian Inheritance in Man, OMIM (TM). Center for Medical Genetics, Johns Hopkins University (Baltimore, MD) and National Center for Biotechnology Information, National Library of Medicine (Bethesda, MD)
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    • (1996)
  • 7
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    • Fetal nuchal translucency: A need to understand the physiological basis
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    • End-result of routine ultrasound screening for congenital anomalies : The Belgian Multicentric study 1984-1992
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.