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Response to Hall et al.
Chong, Jessica X; Talbot, Jared C; Teets, Emily M; Previs, Samantha; Martin, Brit L; Shively, Kathryn M; Marvin, Colby T; Aylsworth, Arthur S; Saadeh-Haddad, Reem; Schatz, Ulrich A; Inzana, Francesca; Ben-Omran, Tawfeg; Almusafri, Fatima; Al-Mulla, Mariam; Buckingham, Kati J; Harel, Tamar; Mor-Shaked, Hagar; Radhakrishnan, Periyasamy; Girisha, Katta M; Nayak, Shalini S; Shukla, Anju; Dieterich, Klaus; Faure, Julien; Rendu, John; Capri, Yline; Latypova, Xenia; Nickerson, Deborah A; Warshaw, David; Janssen, Paul M; Amacher, Sharon L; Bamshad, Michael J.
Afiliação
  • Chong JX; Division of Genetic Medicine, Department of Pediatrics, University of Washington, Seattle, WA 98195, USA; Brotman-Baty Institute, Seattle, WA 98195, USA.
  • Talbot JC; Department of Molecular Genetics, The Ohio State University, Columbus, OH 43210, USA; Center for Muscle Health and Neuromuscular Disorders, Columbus OH 43210, USA. Electronic address: jared.talbot@maine.edu.
  • Teets EM; Department of Molecular Genetics, The Ohio State University, Columbus, OH 43210, USA.
  • Previs S; Department of Molecular Physiology and Biophysics, University of Vermont, Burlington, VT 05405, USA.
  • Martin BL; Department of Physiology and Cell Biology, The Ohio State University, Columbus, OH 43210, USA.
  • Shively KM; Division of Genetic Medicine, Department of Pediatrics, University of Washington, Seattle, WA 98195, USA.
  • Marvin CT; Division of Genetic Medicine, Department of Pediatrics, University of Washington, Seattle, WA 98195, USA.
  • Aylsworth AS; Departments of Pediatrics and Genetics, University of North Carolina, Chapel Hill, NC 27599, USA.
  • Saadeh-Haddad R; Division of Genetics, Department of Pediatrics, Medstar Georgetown University Hospital, Washington, DC 20007, USA.
  • Schatz UA; Human Genetics, Medical University, Innsbruck 6020, Austria.
  • Inzana F; Genetic Counseling Service, Department of Pediatrics, Regional Hospital of Bolzano, Bolzano 39100, Italy.
  • Ben-Omran T; Division of Genetic and Genomic Medicine, Sidra Medicine and Hamad Medical Corporation, PO Box 3050, Doha, Qatar.
  • Almusafri F; Division of Genetic and Genomic Medicine, Sidra Medicine and Hamad Medical Corporation, PO Box 3050, Doha, Qatar.
  • Al-Mulla M; Division of Genetic and Genomic Medicine, Sidra Medicine and Hamad Medical Corporation, PO Box 3050, Doha, Qatar.
  • Buckingham KJ; Division of Genetic Medicine, Department of Pediatrics, University of Washington, Seattle, WA 98195, USA.
  • Harel T; Department of Genetics, Hadassah-Hebrew University Medical Center, Jerusalem 91120, Israel.
  • Mor-Shaked H; Department of Genetics, Hadassah-Hebrew University Medical Center, Jerusalem 91120, Israel.
  • Radhakrishnan P; Department of Medical Genetics, Kasturba Medical College, Manipal, Manipal Academy of Higher Education, Manipal 576104, India.
  • Girisha KM; Department of Medical Genetics, Kasturba Medical College, Manipal, Manipal Academy of Higher Education, Manipal 576104, India.
  • Nayak SS; Department of Medical Genetics, Kasturba Medical College, Manipal, Manipal Academy of Higher Education, Manipal 576104, India.
  • Shukla A; Department of Medical Genetics, Kasturba Medical College, Manipal, Manipal Academy of Higher Education, Manipal 576104, India.
  • Dieterich K; Department of Medical Genetics, CHU Grenoble Alpes, Génétique Médicale, Grenoble 38700, France; Université Grenoble Alpes, Inserm, U1216, Grenoble Institut des Neurosciences, Grenoble 38706, France.
  • Faure J; Université Grenoble Alpes, Inserm, U1216, Grenoble Institut des Neurosciences, Grenoble 38706, France; Biochimie Génétique et Moléculaire, CHU Grenoble Alpes, Grenoble 38700, France.
  • Rendu J; Université Grenoble Alpes, Inserm, U1216, Grenoble Institut des Neurosciences, Grenoble 38706, France; Biochimie Génétique et Moléculaire, CHU Grenoble Alpes, Grenoble 38700, France.
  • Capri Y; Department of Genetics, APHP-Robert DEBRE University Hospital, UF Génétique clinique, Paris 75019, France.
  • Latypova X; Université Grenoble Alpes, Inserm, U1216, Grenoble Institut des Neurosciences, Grenoble 38706, France; Biochimie Génétique et Moléculaire, CHU Grenoble Alpes, Grenoble 38700, France.
  • Nickerson DA; Brotman-Baty Institute, Seattle, WA 98195, USA; Department of Genome Sciences, University of Washington, Seattle, WA 98195, USA.
  • Warshaw D; Department of Molecular Physiology and Biophysics, University of Vermont, Burlington, VT 05405, USA.
  • Janssen PM; Department of Physiology and Cell Biology, The Ohio State University, Columbus, OH 43210, USA.
  • Amacher SL; Department of Molecular Genetics, The Ohio State University, Columbus, OH 43210, USA; Center for Muscle Health and Neuromuscular Disorders, Columbus OH 43210, USA; Dept of Biological Chemistry and Pharmacology, The Ohio State University, Columbus, OH 43210, USA; Center for RNA Biology, The Ohio Stat
  • Bamshad MJ; Division of Genetic Medicine, Department of Pediatrics, University of Washington, Seattle, WA 98195, USA; Brotman-Baty Institute, Seattle, WA 98195, USA; Department of Genome Sciences, University of Washington, Seattle, WA 98195, USA; Seattle Children's Hospital, Seattle, WA 98105, USA. Electronic a
Am J Hum Genet ; 107(6): 1188-1189, 2020 12 03.
Article em En | MEDLINE | ID: mdl-33275912
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Artrogripose / Anormalidades Musculoesqueléticas Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article
Texto completo
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Artrogripose / Anormalidades Musculoesqueléticas Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article