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Maternal Hypomethylation of KvDMR in a Monozygotic Male Twin Pair Discordant for Beckwith-Wiedemann Syndrome.
Elalaoui, S C; Garin, I; Sefiani, A; Perez de Nanclares, G.
Affiliation
  • Elalaoui SC; Département de Génétique Médicale, Institut National d'Hygiène, Rabat, Morocco ; Centre de Génomique Humaine, Faculté de Médecine et de Pharmacie, Université Mohammed V Souissi, Rabat, Morocco.
  • Garin I; Molecular (Epi)Genetics Laboratory, Hospital Universitario-Araba-Txagorritxu, Vitoria-Gazteiz, Spain.
  • Sefiani A; Département de Génétique Médicale, Institut National d'Hygiène, Rabat, Morocco ; Centre de Génomique Humaine, Faculté de Médecine et de Pharmacie, Université Mohammed V Souissi, Rabat, Morocco.
  • Perez de Nanclares G; Molecular (Epi)Genetics Laboratory, Hospital Universitario-Araba-Txagorritxu, Vitoria-Gazteiz, Spain.
Mol Syndromol ; 5(1): 41-6, 2014 Jan.
Article in En | MEDLINE | ID: mdl-24550765
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: Mol Syndromol Year: 2014 Document type: Article Affiliation country: Marruecos Country of publication: Suiza
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: Mol Syndromol Year: 2014 Document type: Article Affiliation country: Marruecos Country of publication: Suiza