Malformations, genetic abnormalities, and Wilms tumor.

Dumoucel, S; Gauthier-Villars, M; Stoppa-Lyonnet, D; Parisot, P; Brisse, H; Philippe-Chomette, P; Sarnacki, S; Boccon-Gibod, L; Rossignol, S; Baumann, C; Aerts, I; Bourdeaut, F; Doz, F; Orbach, D; Pacquement, H; Michon, J; Schleiermacher, G

Dumoucel, S; Gauthier-Villars, M; Stoppa-Lyonnet, D; Parisot, P; Brisse, H; Philippe-Chomette, P; Sarnacki, S; Boccon-Gibod, L; Rossignol, S; Baumann, C; Aerts, I; Bourdeaut, F; Doz, F; Orbach, D; Pacquement, H; Michon, J; Schleiermacher, G.

Affiliation

Dumoucel S; Department of Pediatric Oncology, Institut Curie, Paris, France.

Pediatr Blood Cancer ; 61(1): 140-4, 2014 Jan.

Article in En | MEDLINE | ID: mdl-23970395

Subject(s)

Abnormalities, Multiple; Wilms Tumor/complications; Wilms Tumor/genetics; Child; Child, Preschool; Female; Genetic Predisposition to Disease; Humans; Male; Retrospective Studies; Syndrome; Wilms Tumor/mortality

Key words

WT1; Wilms tumor; genetic abnormality; hemihypertrophy; nephroblastoma; predisposition syndrome

Fulltext

XML

PubMed Links

Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Abnormalities, Multiple / Wilms Tumor Type of study: Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Child / Child, preschool / Female / Humans / Male Language: En Journal: Pediatr Blood Cancer Journal subject: HEMATOLOGIA / NEOPLASIAS / PEDIATRIA Year: 2014 Type: Article Affiliation country: France

Fulltext

XML

PubMed Links

Search on Google