Novel PTCH1 Mutation in a Young Child With Gorlin Syndrome and Medulloblastoma.

Gloude, Nicholas J; Yoon, Janet M; Crawford, John R

Gloude, Nicholas J; Yoon, Janet M; Crawford, John R.

Afiliación

Gloude NJ; Division of Hematology-Oncology, Department of Pediatrics, Rady Children's Hospital-San Diego, University of California, San Diego, San Diego, California.
Yoon JM; Division of Hematology-Oncology, Department of Pediatrics, Rady Children's Hospital-San Diego, University of California, San Diego, San Diego, California.
Crawford JR; Division of Hematology-Oncology, Department of Pediatrics, Rady Children's Hospital-San Diego, University of California, San Diego, San Diego, California.

Pediatr Blood Cancer ; 63(6): 1128-9, 2016 Jun.

Article en En | MEDLINE | ID: mdl-26840755

Asunto(s)

Síndrome del Nevo Basocelular/genética; Neoplasias Cerebelosas/genética; Meduloblastoma/genética; Receptores de Superficie Celular/genética; Preescolar; Humanos; Masculino; Mutación; Receptores Patched; Receptor Patched-1

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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Síndrome del Nevo Basocelular / Neoplasias Cerebelosas / Receptores de Superficie Celular / Meduloblastoma Límite: Child, preschool / Humans / Male Idioma: En Revista: Pediatr Blood Cancer Asunto de la revista: HEMATOLOGIA / NEOPLASIAS / PEDIATRIA Año: 2016 Tipo del documento: Article

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