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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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 28190301 AccessLevel: 2 PubTypeId: unknown PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Cornelia de Lange syndrome and molecular implications of the cohesin complex: Abstracts from the 7th biennial scientific and educational symposium 2016. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Kline+AD%22">Kline AD</searchLink>; Harvey Institute for Human Genetics, Greater Baltimore Medical Center, Baltimore, Maryland.<br /><searchLink fieldCode="AU" term="%22Krantz+ID%22">Krantz ID</searchLink>; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.; Perelman School of Medicine at The University of Pennsylvania, Philadelphia, Pennsylvania.<br /><searchLink fieldCode="AU" term="%22Deardorff+MA%22">Deardorff MA</searchLink>; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.; Perelman School of Medicine at The University of Pennsylvania, Philadelphia, Pennsylvania.<br /><searchLink fieldCode="AU" term="%22Shirahige+K%22">Shirahige K</searchLink>; Institute of Molecular and Cellular Biosciences, The University of Tokyo, and CREST, Japanese Science and Technology Agency, Tokyo, Japan.<br /><searchLink fieldCode="AU" term="%22Dorsett+D%22">Dorsett D</searchLink>; Edward A. Doisy Department of Biochemistry and Molecular Biology, Saint Louis University School of Medicine, Saint Louis, Missouri.<br /><searchLink fieldCode="AU" term="%22Gerton+JL%22">Gerton JL</searchLink>; Stowers Institute for Medical Research, Department of Biochemistry and Molecular Biology, University of Kansas School of Medicine, Kansas City, Missouri.<br /><searchLink fieldCode="AU" term="%22Wu+M%22">Wu M</searchLink>; Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, New York.<br /><searchLink fieldCode="AU" term="%22Mehta+D%22">Mehta D</searchLink>; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.<br /><searchLink fieldCode="AU" term="%22Mills+JA%22">Mills JA</searchLink>; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.<br /><searchLink fieldCode="AU" term="%22Carrico+CS%22">Carrico CS</searchLink>; Communication Sciences and Disorders, Elmhurst College, Elmhurst, Illinois.<br /><searchLink fieldCode="AU" term="%22Noon+S%22">Noon S</searchLink>; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.<br /><searchLink fieldCode="AU" term="%22Herrera+PS%22">Herrera PS</searchLink>; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.<br /><searchLink fieldCode="AU" term="%22Horsfield+JA%22">Horsfield JA</searchLink>; Department of Pathology, Dunedin School of Medicine, University of Otago, Dunedin, New Zealand.<br /><searchLink fieldCode="AU" term="%22Bettale+C%22">Bettale C</searchLink>; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.<br /><searchLink fieldCode="AU" term="%22Morgan+J%22">Morgan J</searchLink>; Sanford Children's Health Research Center, Sanford Research, Sioux Falls, South Dakota.<br /><searchLink fieldCode="AU" term="%22Huisman+SA%22">Huisman SA</searchLink>; Academic Medical Center, University of Amsterdam, Amsterdam, Netherlands.<br /><searchLink fieldCode="AU" term="%22Moss+J%22">Moss J</searchLink>; Cerebra Centre for Neurodevelopmental Disorders, School of Psychology, University of Birmingham, Birmingham, UK.<br /><searchLink fieldCode="AU" term="%22McCleery+J%22">McCleery J</searchLink>; Pyramid Educational Consultants, Clinical Research and Development, Newark, Delaware.<br /><searchLink fieldCode="AU" term="%22Grados+M%22">Grados M</searchLink>; Department of Psychiatry and Behavioral Sciences, Baltimore, Maryland.<br /><searchLink fieldCode="AU" term="%22Hansen+BD%22">Hansen BD</searchLink>; Department of Counseling Psychology and Special Education, Brigham Young University, Provo, Utah.<br /><searchLink fieldCode="AU" term="%22Srivastava+S%22">Srivastava S</searchLink>; Child Neurology and Developmental Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.<br /><searchLink fieldCode="AU" term="%22Taylor-Snell+E%22">Taylor-Snell E</searchLink>; Florida and Virgin Islands Deaf-Blind Collaborative, University of Florida Health Sciences Center, Gainesville, Florida.<br /><searchLink fieldCode="AU" term="%22Kerr+LM%22">Kerr LM</searchLink>; Division of Pediatric Neurology, Department of Pediatrics, University of Utah Medical Center, Salt Lake City, Utah.<br /><searchLink fieldCode="AU" term="%22Katz+O%22">Katz O</searchLink>; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.<br /><searchLink fieldCode="AU" term="%22Calof+AL%22">Calof AL</searchLink>; Departments of Anatomy and Neurobiology, Developmental and Cell Biology, and the Center for Complex Biological Systems, University of California, Irvine, California.<br /><searchLink fieldCode="AU" term="%22Musio+A%22">Musio A</searchLink>; Istituto di Ricerca Genetica e Biomedica, Consiglio Nazionale delle Ricerche, Pisa, Italy.<br /><searchLink fieldCode="AU" term="%22Egense+A%22">Egense A</searchLink>; Division of Human Genetics, Department of Pediatrics, University of Maryland Medical Center, Baltimore, Maryland.<br /><searchLink fieldCode="AU" term="%22Haaland+RE%22">Haaland RE</searchLink>; Cornelia de Lange Syndrome Foundation, Avon, Connecticut. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22101235741%22">American journal of medical genetics. Part A</searchLink> [Am J Med Genet A] 2017 May; Vol. 173 (5), pp. 1172-1185. <i>Date of Electronic Publication: </i>2017 Feb 12. – Name: TypePub Label: Publication Type Group: TypPub Data: Conference Proceedings – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Wiley-Blackwell%22">Wiley-Blackwell </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>101235741 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1552-4833 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2215524825%22">15524825 </searchLink><i>NLM ISO Abbreviation: </i>Am J Med Genet A <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=28190301 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1002/ajmg.a.38161 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 1172 Titles: – TitleFull: Cornelia de Lange syndrome and molecular implications of the cohesin complex: Abstracts from the 7th biennial scientific and educational symposium 2016. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Kline AD – PersonEntity: Name: NameFull: Krantz ID – PersonEntity: Name: NameFull: Deardorff MA – PersonEntity: Name: NameFull: Shirahige K – PersonEntity: Name: NameFull: Dorsett D – PersonEntity: Name: NameFull: Gerton JL – PersonEntity: Name: NameFull: Wu M – PersonEntity: Name: NameFull: Mehta D – PersonEntity: Name: NameFull: Mills JA – PersonEntity: Name: NameFull: Carrico CS – PersonEntity: Name: NameFull: Noon S – PersonEntity: Name: NameFull: Herrera PS – PersonEntity: Name: NameFull: Horsfield JA – PersonEntity: Name: NameFull: Bettale C – PersonEntity: Name: NameFull: Morgan J – PersonEntity: Name: NameFull: Huisman SA – PersonEntity: Name: NameFull: Moss J – PersonEntity: Name: NameFull: McCleery J – PersonEntity: Name: NameFull: Grados M – PersonEntity: Name: NameFull: Hansen BD – PersonEntity: Name: NameFull: Srivastava S – PersonEntity: Name: NameFull: Taylor-Snell E – PersonEntity: Name: NameFull: Kerr LM – PersonEntity: Name: NameFull: Katz O – PersonEntity: Name: NameFull: Calof AL – PersonEntity: Name: NameFull: Musio A – PersonEntity: Name: NameFull: Egense A – PersonEntity: Name: NameFull: Haaland RE IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 05 Text: 2017 May Type: published Y: 2017 Identifiers: – Type: issn-electronic Value: 1552-4833 Numbering: – Type: volume Value: 173 – Type: issue Value: 5 Titles: – TitleFull: American journal of medical genetics. Part A Type: main |
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