Otopalatodigital Syndrome Type I: Novel Characteristics and Prenatal Manifestations in two Siblings.

Joksic, I; Cuturilo, G; Jurisic, A; Djuricic, S; Peterlin, B; Mijovic, M; Karadzov, Orlic N; Egic, A; Milovanovic, Z

Joksic, I; Cuturilo, G; Jurisic, A; Djuricic, S; Peterlin, B; Mijovic, M; Karadzov, Orlic N; Egic, A; Milovanovic, Z.

Afiliación

Joksic I; Gynecology and Obstetrics Clinic "Narodni Front", Belgrade, Serbia.
Cuturilo G; Faculty of Medicine, University of Belgrade, Belgrade, Serbia.
Jurisic A; University Children's Hospital, Belgrade, Serbia.
Djuricic S; Gynecology and Obstetrics Clinic "Narodni Front", Belgrade, Serbia.
Peterlin B; Faculty of Medicine, University of Belgrade, Belgrade, Serbia.
Mijovic M; Department of Pathology, Institute for Mother and Child Health Care "Dr Vukan Cupic", Belgrade, Serbia.
Karadzov ON; School of Medicine, University of Banjaluka, Banjaluka, Bosnia and Herzegovina.
Egic A; Clinical Institute for Genomic Medicine, Ljubljana, Slovenia.
Milovanovic Z; Faculty of Medicine, University of Belgrade, Belgrade, Serbia.

Balkan J Med Genet ; 22(2): 83-88, 2019 Dec.

Article en En | MEDLINE | ID: mdl-31942422

Palabras clave

Autopsy; Filamin A gene (FLNA); Microphtalmia; Otoplalatodigital syndrome type I (OPD type I); Prenatal diagnosis (PND)

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Balkan J Med Genet Año: 2019 Tipo del documento: Article Pais de publicación: Polonia

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