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CpG Methylation, a Parent-of-Origin Effect for Maternal-Biased Transmission of Congenital Myotonic Dystrophy.
Barbé, Lise; Lanni, Stella; López-Castel, Arturo; Franck, Silvie; Spits, Claudia; Keymolen, Kathelijn; Seneca, Sara; Tomé, Stephanie; Miron, Ioana; Letourneau, Julie; Liang, Minggao; Choufani, Sanaa; Weksberg, Rosanna; Wilson, Michael D; Sedlacek, Zdenek; Gagnon, Cynthia; Musova, Zuzana; Chitayat, David; Shannon, Patrick; Mathieu, Jean; Sermon, Karen; Pearson, Christopher E.
Afiliación
  • Barbé L; Department for Reproduction and Genetics, Vrije Universiteit Brussel, Brussels 1090, Belgium.
  • Lanni S; Genetics & Genome Biology, The Hospital for Sick Children, Toronto, ON M5G 0A4, Canada.
  • López-Castel A; Genetics & Genome Biology, The Hospital for Sick Children, Toronto, ON M5G 0A4, Canada.
  • Franck S; Department for Reproduction and Genetics, Vrije Universiteit Brussel, Brussels 1090, Belgium.
  • Spits C; Department for Reproduction and Genetics, Vrije Universiteit Brussel, Brussels 1090, Belgium.
  • Keymolen K; Centre for Medical Genetics, Universitair Ziekenhuis Brussel, Brussels 1090, Belgium.
  • Seneca S; Centre for Medical Genetics, Universitair Ziekenhuis Brussel, Brussels 1090, Belgium.
  • Tomé S; Genetics & Genome Biology, The Hospital for Sick Children, Toronto, ON M5G 0A4, Canada.
  • Miron I; The Prenatal Diagnosis and Medical Genetics Program, Department of Obstetrics and Gynecology, University of Toronto, Toronto, ON M5G 1E2, Canada.
  • Letourneau J; Groupe de Recherche Interdisciplinaire sur les Maladies Neuromusculaires, Saguenay, QC 75204, Canada.
  • Liang M; Genetics & Genome Biology, The Hospital for Sick Children, Toronto, ON M5G 0A4, Canada; The Department of Molecular Genetics, University of Toronto, Toronto, ON M5S 1A8, Canada.
  • Choufani S; Genetics & Genome Biology, The Hospital for Sick Children, Toronto, ON M5G 0A4, Canada.
  • Weksberg R; Genetics & Genome Biology, The Hospital for Sick Children, Toronto, ON M5G 0A4, Canada; The Department of Molecular Genetics, University of Toronto, Toronto, ON M5S 1A8, Canada; Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, Toronto, ON M5G 1X8, Canada; Institute of
  • Wilson MD; Genetics & Genome Biology, The Hospital for Sick Children, Toronto, ON M5G 0A4, Canada; The Department of Molecular Genetics, University of Toronto, Toronto, ON M5S 1A8, Canada.
  • Sedlacek Z; Department of Biology and Medical Genetics, Charles University Prague, Prague 128 00, Czech Republic.
  • Gagnon C; Groupe de Recherche Interdisciplinaire sur les Maladies Neuromusculaires, Saguenay, QC 75204, Canada.
  • Musova Z; Department of Biology and Medical Genetics, Charles University Prague, Prague 128 00, Czech Republic.
  • Chitayat D; The Prenatal Diagnosis and Medical Genetics Program, Department of Obstetrics and Gynecology, University of Toronto, Toronto, ON M5G 1E2, Canada; Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, Toronto, ON M5G 1X8, Canada.
  • Shannon P; Department of Pathology and Laboratory Medicine, Mount Sinai Hospital, University of Toronto, Toronto, ON M5G 1X5, Canada.
  • Mathieu J; Groupe de Recherche Interdisciplinaire sur les Maladies Neuromusculaires, Saguenay, QC 75204, Canada.
  • Sermon K; Department for Reproduction and Genetics, Vrije Universiteit Brussel, Brussels 1090, Belgium. Electronic address: karen.sermon@uzbrussel.be.
  • Pearson CE; Genetics & Genome Biology, The Hospital for Sick Children, Toronto, ON M5G 0A4, Canada; The Department of Molecular Genetics, University of Toronto, Toronto, ON M5S 1A8, Canada. Electronic address: cepearson.sickkids@gmail.com.
Am J Hum Genet ; 100(3): 488-505, 2017 Mar 02.
Article en En | MEDLINE | ID: mdl-28257691
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Islas de CpG / Metilación de ADN / Proteína Quinasa de Distrofia Miotónica / Distrofia Miotónica Tipo de estudio: Prognostic_studies Límite: Adolescent / Adult / Child / Female / Humans / Male / Pregnancy Idioma: En Revista: Am J Hum Genet Año: 2017 Tipo del documento: Article País de afiliación: Bélgica
Texto completo
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Islas de CpG / Metilación de ADN / Proteína Quinasa de Distrofia Miotónica / Distrofia Miotónica Tipo de estudio: Prognostic_studies Límite: Adolescent / Adult / Child / Female / Humans / Male / Pregnancy Idioma: En Revista: Am J Hum Genet Año: 2017 Tipo del documento: Article País de afiliación: Bélgica