13q interstitial deletion in a moroccan child with hereditary retinoblastoma and intellectual disability: A case report.

Outtaleb, F Z; Kora, L; Jabrane, G; Serbati, N; El Maaloum, L; Allali, B; El Kettani, A; Dehbi, H

Outtaleb, F Z; Kora, L; Jabrane, G; Serbati, N; El Maaloum, L; Allali, B; El Kettani, A; Dehbi, H.

Afiliación

Outtaleb FZ; Laboratory of Medical Genetics, Ibn Rochd University Hospital of Casablanca, Morocco.
Kora L; Pediatric Ophthalmology Department, Ibn Rochd University Hospital of Casablanca, Morocco.
Jabrane G; Laboratory of Medical Genetics, Ibn Rochd University Hospital of Casablanca, Morocco.
Serbati N; Laboratory of Medical Genetics, Ibn Rochd University Hospital of Casablanca, Morocco.
El Maaloum L; Pediatric Ophthalmology Department, Ibn Rochd University Hospital of Casablanca, Morocco.
Allali B; Pediatric Ophthalmology Department, Ibn Rochd University Hospital of Casablanca, Morocco.
El Kettani A; Pediatric Ophthalmology Department, Ibn Rochd University Hospital of Casablanca, Morocco.
Dehbi H; Laboratory of Medical Genetics, Ibn Rochd University Hospital of Casablanca, Morocco.

Ann Med Surg (Lond) ; 60: 334-337, 2020 Dec.

Article en En | MEDLINE | ID: mdl-33224486

Palabras clave

13q interstitial deletion; Case report; Genetic counseling; Retinoblastoma

Texto completo

Añadir a Mi BVS

Imprimir

XML

PubMed Links

Buscar en Google

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Ann Med Surg (Lond) Año: 2020 Tipo del documento: Article País de afiliación: Marruecos