A newborn with monosomy X in association with corpus callosum agenesis.

Onur Cura, Duygu; Iscan, Burcin; Gursoy, Semra; Guleryuz, Handan; Cankaya, Tufan; Ozturk, Tulay; Giray Bozkaya, Ozlem

Onur Cura, Duygu; Iscan, Burcin; Gursoy, Semra; Guleryuz, Handan; Cankaya, Tufan; Ozturk, Tulay; Giray Bozkaya, Ozlem.

Afiliación

Onur Cura D; Department of Medical Genetics, Faculty of Medicine, Dokuz Eylul University, Balcova 35330, Izmir, Turkey. Electronic address: duyguonur_05@hotmail.com.
Iscan B; Division of Neonatology, Department of Pediatrics, Faculty of Medicine, Dokuz Eylul University, Balcova 35330, Izmir, Turkey.
Gursoy S; Division of Pediatric Genetic Disorders, Department of Pediatrics, Faculty of Medicine, Dokuz Eylul University, Balcova 35330, Izmir, Turkey.
Guleryuz H; Division of Pediatric Radiology, Department of Radiology, Faculty of Medicine, Dokuz Eylul University, Balcova 35330, Izmir, Turkey.
Cankaya T; Department of Medical Genetics, Faculty of Medicine, Dokuz Eylul University, Balcova 35330, Izmir, Turkey.
Ozturk T; Division of Pediatric Radiology, Department of Radiology, Faculty of Medicine, Dokuz Eylul University, Balcova 35330, Izmir, Turkey.
Giray Bozkaya O; Department of Medical Genetics, Faculty of Medicine, Dokuz Eylul University, Balcova 35330, Izmir, Turkey; Division of Pediatric Genetic Disorders, Department of Pediatrics, Faculty of Medicine, Dokuz Eylul University, Balcova 35330, Izmir, Turkey.

Pediatr Neonatol ; 58(5): 455-457, 2017 10.

Article en En | MEDLINE | ID: mdl-28117231

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Revista: Pediatr Neonatol Año: 2017 Tipo del documento: Article Pais de publicación: Singapur

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