Prenatal ultrasound diagnosis in 51 cases of holoprosencephaly: Craniofacial anatomy, associated malformations, and genetics

Cleft Palate-Craniofacial Journal

Volumn 47, Issue 1, 2010, Pages 15-21

  Wenghoefer, M ^a   Ettema, Anke M ^c   Sina, F ^a   Geipel, A ^a   Kuijpers Jagtman, A M ^b   Hansmann, H ^a   Borstlap, W A ^c   Berge S ^c  

^a UNIVERSITY OF BONN   (Germany)

^b RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^c RADBOUD UNIVERSITY NIJMEGEN   (Netherlands)

Author keywords

Holoprosencephaly; HPE; Prenatal ultrasound

Indexed keywords

ADULT; ARTICLE; AUTOPSY; CHROMOSOME ABERRATION; CRANIOFACIAL MALFORMATION; CRANIOFACIAL MORPHOLOGY; FEMALE; FETUS; GENETIC ANALYSIS; GESTATIONAL AGE; HOLOPROSENCEPHALY; HUMAN; HUMAN TISSUE; MAJOR CLINICAL STUDY; MALE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; TRISOMY 13; ULTRASOUND;

ADOLESCENT; ADULT; CHROMOSOME DISORDERS; CONGENITAL ABNORMALITIES; CRANIOFACIAL ABNORMALITIES; FEMALE; GERMANY; HOLOPROSENCEPHALY; HUMANS; INFANT, NEWBORN; KARYOTYPING; MALE; PREGNANCY; PREGNANCY TRIMESTER, SECOND; ULTRASONOGRAPHY, PRENATAL; YOUNG ADULT;

EID: 75649137332     PISSN: 10556656     EISSN: 15451569     Source Type: Journal    
DOI: 10.1597/08-036.1     Document Type: Article

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