Prenatal diagnosis, phenotypic and obstetric characteristics of holoprosencephaly

Fetal Diagnosis and Therapy

Volumn 20, Issue 3, 2005, Pages 161-166

  Joó, Gábor J ^a,b   Beke, Artúr ^a   Papp, Csaba ^a   Tóth Pál, Erno ^a   Szigeti, Zsanett ^a   Bán, Zoltán ^a   Papp, Zoltán ^a  

^a National Institute of Oncology   (Hungary)

^b SEMMELWEIS UNIVERSITY OF MEDICINE   (Hungary)

Author keywords

Accompanying malformations; Holoprosencephaly; Patient's history; Prenataldiagnosis

Indexed keywords

ARTICLE; CENTRAL NERVOUS SYSTEM; CRANIOFACIAL MALFORMATION; DISEASE ASSOCIATION; FEMALE; FETUS; FETUS MALFORMATION; HOLOPROSENCEPHALY; HUMAN; MAJOR CLINICAL STUDY; MALE; PHENOTYPE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; PROGNOSIS; RECURRENT DISEASE;

ADULT; CENTRAL NERVOUS SYSTEM; DISEASES IN TWINS; FEMALE; HOLOPROSENCEPHALY; HUMANS; MALE; MATERNAL AGE; MEDICAL RECORDS; PHENOTYPE; PREGNANCY; PREGNANCY TRIMESTER, FIRST; RETROSPECTIVE STUDIES; ULTRASONOGRAPHY, PRENATAL;

EID: 17844391292     PISSN: 10153837     EISSN: None     Source Type: Journal    
DOI: 10.1159/000083897     Document Type: Article

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