Should determination of the karyotype be systematic for all malformations detected by obstetrical ultrasound?

Prenatal Diagnosis

Volumn 25, Issue 7, 2005, Pages 567-573

  Staebler, M ^a   Donner, C ^b   Van Regemorter, N ^b   Duprez, L ^b   De Maertelaer, V ^c   Devreker, F ^b   Avni, F ^b  

^a HOP UNIV DES ENFANTS REINE FABIOLA   (Belgium)

^b ERASME HOSPITAL   (Belgium)

^c UNIVERSITÉ LIBRE DE BRUXELLES   (Belgium)

Author keywords

Isolated and multiple fetal malformations; Karyotype; Low risk pregnancy; Prenatal ultrasound

Indexed keywords

ARTICLE; CHROMOSOME ANALYSIS; CYSTIC ADENOMATOID MALFORMATION; FETUS; FETUS ECHOGRAPHY; FETUS MALFORMATION; GASTROSCHISIS; HUMAN; HYDRONEPHROSIS; KARYOTYPE; LUNG SEQUESTRATION; MAJOR CLINICAL STUDY; MECONIUM PERITONITIS; MULTICYSTIC DYSPLASTIC KIDNEY; PRIORITY JOURNAL; VERTEBRA MALFORMATION;

ABNORMALITIES, MULTIPLE; ADOLESCENT; ADULT; BELGIUM; CHROMOSOME ABERRATIONS; FEMALE; HUMANS; KARYOTYPING; MEDICAL HISTORY TAKING; PREDICTIVE VALUE OF TESTS; PREGNANCY; PREGNANCY TRIMESTER, SECOND; PREGNANCY TRIMESTER, THIRD; ULTRASONOGRAPHY, PRENATAL;

EID: 23244457216     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/pd.1187     Document Type: Article

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