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CNTN6 copy number variations: Uncertain clinical significance in individuals with neurodevelopmental disorders.

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Title: CNTN6 copy number variations: Uncertain clinical significance in individuals with neurodevelopmental disorders.
Authors: Repnikova EA; The Division of Clinical Genetics and Genomics Laboratories, Children's Mercy Hospital Kansas City, Kansas City, MO, 64108 USA; University Missouri-Kansas City School of Medicine, Kansas City, MO, 64108, USA. Electronic address: erepnikova@cmh.edu., Lyalin DA; The Division of Clinical Genetics and Genomics Laboratories, Children's Mercy Hospital Kansas City, Kansas City, MO, 64108 USA., McDonald K; Department of Pediatrics, Nationwide Children's Hospital, Columbus, OH, 43205, USA., Astbury C; Cytogenetics and Molecular Genetics Laboratory, Department of Pathology and Laboratory Medicine, Nationwide Children's Hospital, Columbus, OH, 43205, USA., Hansen-Kiss E; Department of Pediatrics, Nationwide Children's Hospital, Columbus, OH, 43205, USA; Center for Molecular and Human Genetics, The Research Institute at Nationwide Children's Hospital, Columbus, OH, 43205, USA., Cooley LD; The Division of Clinical Genetics and Genomics Laboratories, Children's Mercy Hospital Kansas City, Kansas City, MO, 64108 USA; University Missouri-Kansas City School of Medicine, Kansas City, MO, 64108, USA., Pfau R; Cytogenetics and Molecular Genetics Laboratory, Department of Pathology and Laboratory Medicine, Nationwide Children's Hospital, Columbus, OH, 43205, USA; The Ohio State University College of Medicine, Columbus, OH, 43210, USA., Herman GE; Department of Pediatrics, Nationwide Children's Hospital, Columbus, OH, 43205, USA; Center for Molecular and Human Genetics, The Research Institute at Nationwide Children's Hospital, Columbus, OH, 43205, USA; The Ohio State University College of Medicine, Columbus, OH, 43210, USA., Pyatt RE; Cytogenetics and Molecular Genetics Laboratory, Department of Pathology and Laboratory Medicine, Nationwide Children's Hospital, Columbus, OH, 43205, USA., Hickey SE; Department of Pediatrics, Nationwide Children's Hospital, Columbus, OH, 43205, USA; The Ohio State University College of Medicine, Columbus, OH, 43210, USA. Electronic address: scott.hickey@nationwidechildrens.org.
Source: European journal of medical genetics [Eur J Med Genet] 2020 Jan; Vol. 63 (1), pp. 103636. Date of Electronic Publication: 2019 Mar 02.
Publication Type: Journal Article
Journal Info: Publisher: Elsevier Country of Publication: Netherlands NLM ID: 101247089 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1878-0849 (Electronic) Linking ISSN: 17697212 NLM ISO Abbreviation: Eur J Med Genet Subsets: MEDLINE
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  Data: CNTN6 copy number variations: Uncertain clinical significance in individuals with neurodevelopmental disorders.
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  Data: <searchLink fieldCode="AU" term="%22Repnikova+EA%22">Repnikova EA</searchLink>; The Division of Clinical Genetics and Genomics Laboratories, Children's Mercy Hospital Kansas City, Kansas City, MO, 64108 USA; University Missouri-Kansas City School of Medicine, Kansas City, MO, 64108, USA. Electronic address: erepnikova@cmh.edu.<br /><searchLink fieldCode="AU" term="%22Lyalin+DA%22">Lyalin DA</searchLink>; The Division of Clinical Genetics and Genomics Laboratories, Children's Mercy Hospital Kansas City, Kansas City, MO, 64108 USA.<br /><searchLink fieldCode="AU" term="%22McDonald+K%22">McDonald K</searchLink>; Department of Pediatrics, Nationwide Children's Hospital, Columbus, OH, 43205, USA.<br /><searchLink fieldCode="AU" term="%22Astbury+C%22">Astbury C</searchLink>; Cytogenetics and Molecular Genetics Laboratory, Department of Pathology and Laboratory Medicine, Nationwide Children's Hospital, Columbus, OH, 43205, USA.<br /><searchLink fieldCode="AU" term="%22Hansen-Kiss+E%22">Hansen-Kiss E</searchLink>; Department of Pediatrics, Nationwide Children's Hospital, Columbus, OH, 43205, USA; Center for Molecular and Human Genetics, The Research Institute at Nationwide Children's Hospital, Columbus, OH, 43205, USA.<br /><searchLink fieldCode="AU" term="%22Cooley+LD%22">Cooley LD</searchLink>; The Division of Clinical Genetics and Genomics Laboratories, Children's Mercy Hospital Kansas City, Kansas City, MO, 64108 USA; University Missouri-Kansas City School of Medicine, Kansas City, MO, 64108, USA.<br /><searchLink fieldCode="AU" term="%22Pfau+R%22">Pfau R</searchLink>; Cytogenetics and Molecular Genetics Laboratory, Department of Pathology and Laboratory Medicine, Nationwide Children's Hospital, Columbus, OH, 43205, USA; The Ohio State University College of Medicine, Columbus, OH, 43210, USA.<br /><searchLink fieldCode="AU" term="%22Herman+GE%22">Herman GE</searchLink>; Department of Pediatrics, Nationwide Children's Hospital, Columbus, OH, 43205, USA; Center for Molecular and Human Genetics, The Research Institute at Nationwide Children's Hospital, Columbus, OH, 43205, USA; The Ohio State University College of Medicine, Columbus, OH, 43210, USA.<br /><searchLink fieldCode="AU" term="%22Pyatt+RE%22">Pyatt RE</searchLink>; Cytogenetics and Molecular Genetics Laboratory, Department of Pathology and Laboratory Medicine, Nationwide Children's Hospital, Columbus, OH, 43205, USA.<br /><searchLink fieldCode="AU" term="%22Hickey+SE%22">Hickey SE</searchLink>; Department of Pediatrics, Nationwide Children's Hospital, Columbus, OH, 43205, USA; The Ohio State University College of Medicine, Columbus, OH, 43210, USA. Electronic address: scott.hickey@nationwidechildrens.org.
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  Data: <searchLink fieldCode="JN" term="%22101247089%22">European journal of medical genetics</searchLink> [Eur J Med Genet] 2020 Jan; Vol. 63 (1), pp. 103636. <i>Date of Electronic Publication: </i>2019 Mar 02.
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        Value: 10.1016/j.ejmg.2019.02.008
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              Text: 2020 Jan
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