De Novo Trisomy 1q10q23.3 Mosaicism Causes Microcephaly, Severe Developmental Delay, and Facial Dysmorphic Features but No Cardiac Anomalies.

Lo-A-Njoe, Shirley; van der Veken, Lars T; Vermont, Clementien; Rafael-Croes, Louise; Keizer, Vincent; Hochstenbach, Ron; Knoers, Nine; van Haelst, Mieke M

Lo-A-Njoe, Shirley; van der Veken, Lars T; Vermont, Clementien; Rafael-Croes, Louise; Keizer, Vincent; Hochstenbach, Ron; Knoers, Nine; van Haelst, Mieke M.

Afiliação

Lo-A-Njoe S; Department of Pediatrics, Horacio Oduber Hospital, Oranjestad, Aruba.
van der Veken LT; Department of Genetics, Wilhelmina Children's Hospital, UMC Utrecht, 3584 EA Utrecht, Netherlands.
Vermont C; Department of Pediatrics, Horacio Oduber Hospital, Oranjestad, Aruba.
Rafael-Croes L; Department of Pediatrics, Horacio Oduber Hospital, Oranjestad, Aruba.
Keizer V; Department of Pediatrics, Horacio Oduber Hospital, Oranjestad, Aruba.
Hochstenbach R; Department of Genetics, Wilhelmina Children's Hospital, UMC Utrecht, 3584 EA Utrecht, Netherlands.
Knoers N; Department of Genetics, Wilhelmina Children's Hospital, UMC Utrecht, 3584 EA Utrecht, Netherlands.
van Haelst MM; Department of Genetics, Wilhelmina Children's Hospital, UMC Utrecht, 3584 EA Utrecht, Netherlands.

Case Rep Genet ; 2016: 2861653, 2016.

Article em En | MEDLINE | ID: mdl-26942023

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies Idioma: En Revista: Case Rep Genet Ano de publicação: 2016 Tipo de documento: Article

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