Methylation-associated PHOX2B gene silencing is a rare event in human neuroblastoma.

de Pontual, Loïc; Trochet, Delphine; Bourdeaut, Franck; Thomas, Sophie; Etchevers, Heather; Chompret, Agnes; Minard, Véronique; Valteau, Dominique; Brugieres, Laurence; Munnich, Arnold; Delattre, Olivier; Lyonnet, Stanislas; Janoueix-Lerosey, Isabelle; Amiel, Jeanne

de Pontual, Loïc; Trochet, Delphine; Bourdeaut, Franck; Thomas, Sophie; Etchevers, Heather; Chompret, Agnes; Minard, Véronique; Valteau, Dominique; Brugieres, Laurence; Munnich, Arnold; Delattre, Olivier; Lyonnet, Stanislas; Janoueix-Lerosey, Isabelle; Amiel, Jeanne.

Affiliation

de Pontual L; Unité de Recherches sur les Handicaps Génétiques de l'Enfant INSERM U-781, et Département de Génétique, Université René-Descartes, Faculté de Médecine, Hôpitaux de Paris, Hôpital Necker-Enfants Malades, 149, rue de Sèvres, 75743 Paris Cedex 15, France.

Eur J Cancer ; 43(16): 2366-72, 2007 Nov.

Article in En | MEDLINE | ID: mdl-17765533

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Collection: 01-internacional Database: MEDLINE Main subject: Transcription Factors / Homeodomain Proteins / Genetic Predisposition to Disease / Neuroblastoma Type of study: Prognostic_studies / Risk_factors_studies Limits: Female / Humans / Male Language: En Journal: Eur J Cancer Year: 2007 Document type: Article Affiliation country:

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