Prenatal diagnosis of Roberts syndrome: Two new cases

Prenatal Diagnosis

Volumn 16, Issue 2, 1996, Pages 125-130

  Benzacken, B ^a   Savary, J B ^b   Manouvrier, S ^c   Bucourt, M ^d   Gonzales, J ^a  

^a AVICENNE HOSPITAL   (France)

^b LILLE UNIVERSITY HOSPITAL   (France)

^c HÔPITAL JEAN VERDIER   (France)

^d Serv de Pediat et de Genet Med   (France)

Author keywords

Centromeric; Disjunction; Roberts syndrome; SC phocomelia

Indexed keywords

AMNION CELL; ARTICLE; AUTOPSY; CASE REPORT; CENTROMERE; CONTROLLED STUDY; CYTOGENETICS; CYTOLOGY; FETUS; HUMAN; HUMAN CELL; PRENATAL SCREENING; PRIORITY JOURNAL; ROBERTS SYNDROME; ULTRASOUND;

ADULT; AMNIOCENTESIS; CELLS, CULTURED; CENTROMERE; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; CRANIOFACIAL DYSOSTOSIS; ECTROMELIA; FEMALE; HUMANS; INFANT, NEWBORN; KARYOTYPING; MALE; PREGNANCY; PREGNANCY OUTCOME; SYNDROME;

EID: 0030056904     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-0223(199602)16:2<125::AID-PD822>3.0.CO;2-S     Document Type: Article

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