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Cornelia de Lange syndrome, related disorders, and the Cohesin complex: Abstracts from the 8th biennial scientific and educational symposium 2018.
Kline, Antonie D; Krantz, Ian D; Bando, Masashige; Shirahige, Katsuhiko; Chea, Stephenson; Sakata, Toyonori; Rao, Suhas; Dorsett, Dale; Singh, Vijay Pratap; Gerton, Jennifer L; Horsfield, Julia A; Calof, Anne L; Katz, Olivia; Grados, Marco; Raible, Sarah; Barañano, Kristin; Lyon, Gholson; Musio, Antonio; Carrico, Cheri S; Clemens, Douglas K; Caudill, Patti; Massa, Valentina; McGill, Bryan E; Dommestrup, Aila; O'Connor, Julia; Haaland, Richard E.
Afiliación
  • Kline AD; Department of Pediatrics, Greater Baltimore Medical Center, Harvey Institute for Human Genetics, Baltimore, Maryland.
  • Krantz ID; Division of Human Genetics, The Children's Hospital of Philadelphia.
  • Bando M; Perelman School of Medicine at The University of Pennsylvania, Philadelphia, Pennsylvania.
  • Shirahige K; Laboratory of Genome Structure and Function, Institute of Molecular and Cellular Biosciences, The University of Tokyo, Tokyo, Japan.
  • Chea S; Laboratory of Genome Structure and Function, Institute of Molecular and Cellular Biosciences, The University of Tokyo, Tokyo, Japan.
  • Sakata T; Departments of Anatomy & Neurobiology, Developmental and Cell Biology, and the Center for Complex Biological Systems, University of California, Irvine, California.
  • Rao S; Laboratory of Genome Structure and Function, Institute of Molecular and Cellular Biosciences, The University of Tokyo, Tokyo, Japan.
  • Dorsett D; Department of Structural Biology, Stanford University School of Medicine, Stanford, California.
  • Singh VP; Edward A. Doisy Department of Biochemistry and Molecular Biology, Saint Louis University School of Medicine, Saint Louis, Missouri.
  • Gerton JL; Stowers Institute for Medical Research, and Department of Biochemistry and Molecular Biology, University of Kansas School of Medicine, Kansas City, Missouri.
  • Horsfield JA; Stowers Institute for Medical Research, and Department of Biochemistry and Molecular Biology, University of Kansas School of Medicine, Kansas City, Missouri.
  • Calof AL; Department of Pathology, Dunedin School of Medicine, The University of Otago, Dunedin, New Zealand.
  • Katz O; Departments of Anatomy & Neurobiology, Developmental and Cell Biology, and the Center for Complex Biological Systems, University of California, Irvine, California.
  • Grados M; Division of Human Genetics, The Children's Hospital of Philadelphia.
  • Raible S; Department of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Barañano K; Division of Human Genetics, The Children's Hospital of Philadelphia.
  • Lyon G; Child Neurology and Developmental Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Musio A; Cold Spring Harbor Laboratory, Cold Spring Harbor, New York.
  • Carrico CS; Institute for Genetic and Biologic Research, National Research Council, Pisa, Italy.
  • Clemens DK; Communication Sciences and Disorders, Elmhurst College, Elmhurst, Illinois.
  • Caudill P; Department of Oral Maxillofacial Surgery and Dentistry, Sinai Hospital of Baltimore, and Cross Keys Dental Associates, Baltimore, Maryland.
  • Massa V; Milton J. Dance, Jr. Head & Neck Center, Greater Baltimore Medical Center, Baltimore, Maryland.
  • McGill BE; Department of Health Sciences, University of Milan, Milan, Italy.
  • Dommestrup A; Division of Pediatric and Developmental Neurology, Department of Neurology, Washington University, St. Louis, Missouri.
  • O'Connor J; Kennedy Krieger Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Haaland RE; Kennedy Krieger Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Am J Med Genet A ; 179(6): 1080-1090, 2019 06.
Article en En | MEDLINE | ID: mdl-30874362
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteínas Cromosómicas no Histona / Proteínas de Ciclo Celular / Predisposición Genética a la Enfermedad / Síndrome de Cornelia de Lange / Estudios de Asociación Genética Tipo de estudio: Prognostic_studies Aspecto: Ethics Límite: Humans Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2019 Tipo del documento: Article
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteínas Cromosómicas no Histona / Proteínas de Ciclo Celular / Predisposición Genética a la Enfermedad / Síndrome de Cornelia de Lange / Estudios de Asociación Genética Tipo de estudio: Prognostic_studies Aspecto: Ethics Límite: Humans Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2019 Tipo del documento: Article