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11p15 ICR1 Partial Deletions Associated with IGF2/H19 DMR Hypomethylation and Silver-Russell Syndrome.
Abi Habib, Walid; Brioude, Frederic; Azzi, Salah; Salem, Jennifer; Das Neves, Cristina; Personnier, Claire; Chantot-Bastaraud, Sandra; Keren, Boris; Le Bouc, Yves; Harbison, Madeleine D; Netchine, Irene.
Affiliation
  • Abi Habib W; INSERM, UMR_S 938, CDR Saint-Antoine, Paris, F-75012, France.
  • Brioude F; Sorbonne Universités, UPMC Univ Paris 06, UMR_S 938, CDR Saint-Antoine, Paris, F-75012, France.
  • Azzi S; AP-HP, Hôpital Trousseau, Service d'explorations fonctionnelles endocriniennes, Paris, 75571, France.
  • Salem J; INSERM, UMR_S 938, CDR Saint-Antoine, Paris, F-75012, France.
  • Das Neves C; Sorbonne Universités, UPMC Univ Paris 06, UMR_S 938, CDR Saint-Antoine, Paris, F-75012, France.
  • Personnier C; AP-HP, Hôpital Trousseau, Service d'explorations fonctionnelles endocriniennes, Paris, 75571, France.
  • Chantot-Bastaraud S; INSERM, UMR_S 938, CDR Saint-Antoine, Paris, F-75012, France.
  • Keren B; Sorbonne Universités, UPMC Univ Paris 06, UMR_S 938, CDR Saint-Antoine, Paris, F-75012, France.
  • Le Bouc Y; AP-HP, Hôpital Trousseau, Service d'explorations fonctionnelles endocriniennes, Paris, 75571, France.
  • Harbison MD; Epigenetics Programme, The Babraham Institute, Cambridge, UK.
  • Netchine I; MAGIC Foundation, RSS/SGA Research and Education Fund, Oak Park, Illinois.
Hum Mutat ; 38(1): 105-111, 2017 01.
Article in En | MEDLINE | ID: mdl-27701793
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chromosomes, Human, Pair 11 / Insulin-Like Growth Factor II / Sequence Deletion / Genomic Imprinting / DNA Methylation / Silver-Russell Syndrome / RNA, Long Noncoding Type of study: Prognostic_studies / Risk_factors_studies Limits: Child, preschool / Female / Humans / Male Language: En Journal: Hum Mutat Journal subject: GENETICA MEDICA Year: 2017 Type: Article Affiliation country: France
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chromosomes, Human, Pair 11 / Insulin-Like Growth Factor II / Sequence Deletion / Genomic Imprinting / DNA Methylation / Silver-Russell Syndrome / RNA, Long Noncoding Type of study: Prognostic_studies / Risk_factors_studies Limits: Child, preschool / Female / Humans / Male Language: En Journal: Hum Mutat Journal subject: GENETICA MEDICA Year: 2017 Type: Article Affiliation country: France