A Case With Short Stature, Growth Hormone Deficiency and 46, XX, Xq27-qter Deletion.

Yildirim, Sule; Topaloglu, Naci; Tekin, Mustafa; Silan, Fatma

Yildirim, Sule; Topaloglu, Naci; Tekin, Mustafa; Silan, Fatma.

Afiliación

Yildirim S; Department of Pediatrics, School of Medicine, Çanakkale Onsekiz Mart University, Çanakkale, Turkey.
Topaloglu N; Department of Pediatrics, School of Medicine, Çanakkale Onsekiz Mart University, Çanakkale, Turkey.
Tekin M; Department of Pediatrics, School of Medicine, Çanakkale Onsekiz Mart University, Çanakkale, Turkey.
Silan F; Department of Medical Genetics, School of Medicine, Çanakkale Onsekiz Mart University, Çanakkale, Turkey.

Acta Med Iran ; 55(10): 661-663, 2017 Oct.

Article en En | MEDLINE | ID: mdl-29228534

Asunto(s)

Cromosomas Humanos X/genética; Discapacidades del Desarrollo/genética; Hormona del Crecimiento/deficiencia; Niño; Femenino; Humanos; Cariotipificación; Eliminación de Secuencia

Palabras clave

Deletion; Gene; Growth hormone deficiency; Short stature; X chromosome

Buscar en Google

Imprimir

XML

PubMed Links

Base de datos: MEDLINE Asunto principal: Hormona del Crecimiento / Discapacidades del Desarrollo / Cromosomas Humanos X Límite: Child / Female / Humans Idioma: En Revista: Acta Med Iran Año: 2017 Tipo del documento: Article País de afiliación: Turquía

Buscar en Google

Imprimir

XML

PubMed Links