Prenatal sonographic findings in trisomy 13, 18, 21 and 22: A review of 46 cases

Journal of Reproductive Medicine for the Obstetrician and Gynecologist

Volumn 39, Issue 10, 1994, Pages 781-787

  Seoud, M A F ^a   Alley, D C ^a   Smith, D L ^a   Levy, D L ^a  

^a EASTERN VIRGINIA MEDICAL SCHOOL   (United States)

Author keywords

prenatal diagnosis; trisomy; ultrasonic

Indexed keywords

AMNIOCENTESIS; ARTICLE; CLINICAL FEATURE; FETUS; FETUS ECHOGRAPHY; FETUS KARYOTYPING; HUMAN; MAJOR CLINICAL STUDY; PRENATAL SCREENING; PRIORITY JOURNAL; SECOND TRIMESTER PREGNANCY; TRISOMY; TRISOMY 13; TRISOMY 18; TRISOMY 21; TRISOMY 22;

ADULT; AMNIOCENTESIS; BIOMETRY; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 13; CHROMOSOMES, HUMAN, PAIR 18; CHROMOSOMES, HUMAN, PAIR 21; CHROMOSOMES, HUMAN, PAIR 22; FEMALE; FEMUR; FETAL DISEASES; HEART DEFECTS, CONGENITAL; HUMANS; INTESTINES; KIDNEY PELVIS; MATERNAL AGE; NECK; PREDICTIVE VALUE OF TESTS; PREGNANCY; PREGNANCY TRIMESTER, SECOND; TRISOMY; ULTRASONOGRAPHY, PRENATAL;

EID: 0027970393     PISSN: 00247758     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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