Cornelia de Lange syndrome and molecular implications of the cohesin complex: Abstracts from the 7th biennial scientific and educational symposium 2016.
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| Title: | Cornelia de Lange syndrome and molecular implications of the cohesin complex: Abstracts from the 7th biennial scientific and educational symposium 2016. |
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| Authors: | Kline AD; Harvey Institute for Human Genetics, Greater Baltimore Medical Center, Baltimore, Maryland., Krantz ID; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.; Perelman School of Medicine at The University of Pennsylvania, Philadelphia, Pennsylvania., Deardorff MA; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.; Perelman School of Medicine at The University of Pennsylvania, Philadelphia, Pennsylvania., Shirahige K; Institute of Molecular and Cellular Biosciences, The University of Tokyo, and CREST, Japanese Science and Technology Agency, Tokyo, Japan., Dorsett D; 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, Department of Biochemistry and Molecular Biology, University of Kansas School of Medicine, Kansas City, Missouri., Wu M; Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, New York., Mehta D; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania., Mills JA; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania., Carrico CS; Communication Sciences and Disorders, Elmhurst College, Elmhurst, Illinois., Noon S; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania., Herrera PS; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania., Horsfield JA; Department of Pathology, Dunedin School of Medicine, University of Otago, Dunedin, New Zealand., Bettale C; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania., Morgan J; Sanford Children's Health Research Center, Sanford Research, Sioux Falls, South Dakota., Huisman SA; Academic Medical Center, University of Amsterdam, Amsterdam, Netherlands., Moss J; Cerebra Centre for Neurodevelopmental Disorders, School of Psychology, University of Birmingham, Birmingham, UK., McCleery J; Pyramid Educational Consultants, Clinical Research and Development, Newark, Delaware., Grados M; Department of Psychiatry and Behavioral Sciences, Baltimore, Maryland., Hansen BD; Department of Counseling Psychology and Special Education, Brigham Young University, Provo, Utah., Srivastava S; Child Neurology and Developmental Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland., Taylor-Snell E; Florida and Virgin Islands Deaf-Blind Collaborative, University of Florida Health Sciences Center, Gainesville, Florida., Kerr LM; Division of Pediatric Neurology, Department of Pediatrics, University of Utah Medical Center, Salt Lake City, Utah., Katz O; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania., Calof AL; Departments of Anatomy and Neurobiology, Developmental and Cell Biology, and the Center for Complex Biological Systems, University of California, Irvine, California., Musio A; Istituto di Ricerca Genetica e Biomedica, Consiglio Nazionale delle Ricerche, Pisa, Italy., Egense A; Division of Human Genetics, Department of Pediatrics, University of Maryland Medical Center, Baltimore, Maryland., Haaland RE; Cornelia de Lange Syndrome Foundation, Avon, Connecticut. |
| Source: | American journal of medical genetics. Part A [Am J Med Genet A] 2017 May; Vol. 173 (5), pp. 1172-1185. Date of Electronic Publication: 2017 Feb 12. |
| Publication Type: | Conference Proceedings |
| Journal Info: | Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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