Pericentromeric regions of homozygosity on the X chromosome: Another likely benign population variant.
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| Title: | Pericentromeric regions of homozygosity on the X chromosome: Another likely benign population variant. |
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| Authors: | Barrie ES; The Institute for Genomic Medicine at Nationwide Children's Hospital, Columbus, OH, USA., Li Y; The Institute for Genomic Medicine at Nationwide Children's Hospital, Columbus, OH, USA., Lamb-Thrush D; The Institute for Genomic Medicine at Nationwide Children's Hospital, Columbus, OH, USA; The Ohio State University College of Medicine, Department of Pediatrics, Columbus, OH, USA., Hashimoto S; The Institute for Genomic Medicine at Nationwide Children's Hospital, Columbus, OH, USA; The Ohio State University College of Medicine, Department of Pediatrics, Columbus, OH, USA., Matthews T; The Institute for Genomic Medicine at Nationwide Children's Hospital, Columbus, OH, USA; The Ohio State University College of Medicine, Department of Pediatrics, Columbus, OH, USA., Mouhlas D; The Institute for Genomic Medicine at Nationwide Children's Hospital, Columbus, OH, USA; The Ohio State University College of Medicine, Department of Pediatrics, Columbus, OH, USA., Pyatt R; The Institute for Genomic Medicine at Nationwide Children's Hospital, Columbus, OH, USA; The Ohio State University College of Medicine, Department of Pathology, Columbus, OH, USA., Reshmi SC; The Institute for Genomic Medicine at Nationwide Children's Hospital, Columbus, OH, USA; The Ohio State University College of Medicine, Department of Pathology, Columbus, OH, USA., Gastier-Foster JM; The Institute for Genomic Medicine at Nationwide Children's Hospital, Columbus, OH, USA; The Ohio State University College of Medicine, Department of Pediatrics, Columbus, OH, USA; The Ohio State University College of Medicine, Department of Pathology, Columbus, OH, USA., Pfau R; The Institute for Genomic Medicine at Nationwide Children's Hospital, Columbus, OH, USA; The Ohio State University College of Medicine, Department of Pathology, Columbus, OH, USA., Astbury C; The Institute for Genomic Medicine at Nationwide Children's Hospital, Columbus, OH, USA; The Ohio State University College of Medicine, Department of Pathology, Columbus, OH, USA. Electronic address: astburc@ccf.org. |
| Source: | European journal of medical genetics [Eur J Med Genet] 2018 Jul; Vol. 61 (7), pp. 416-420. Date of Electronic Publication: 2018 Mar 20. |
| 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 |
| Database: | MEDLINE Ultimate |
| FullText | Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 29572065 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Pericentromeric regions of homozygosity on the X chromosome: Another likely benign population variant. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Barrie+ES%22">Barrie ES</searchLink>; The Institute for Genomic Medicine at Nationwide Children's Hospital, Columbus, OH, USA.<br /><searchLink fieldCode="AU" term="%22Li+Y%22">Li Y</searchLink>; The Institute for Genomic Medicine at Nationwide Children's Hospital, Columbus, OH, USA.<br /><searchLink fieldCode="AU" term="%22Lamb-Thrush+D%22">Lamb-Thrush D</searchLink>; The Institute for Genomic Medicine at Nationwide Children's Hospital, Columbus, OH, USA; The Ohio State University College of Medicine, Department of Pediatrics, Columbus, OH, USA.<br /><searchLink fieldCode="AU" term="%22Hashimoto+S%22">Hashimoto S</searchLink>; The Institute for Genomic Medicine at Nationwide Children's Hospital, Columbus, OH, USA; The Ohio State University College of Medicine, Department of Pediatrics, Columbus, OH, USA.<br /><searchLink fieldCode="AU" term="%22Matthews+T%22">Matthews T</searchLink>; The Institute for Genomic Medicine at Nationwide Children's Hospital, Columbus, OH, USA; The Ohio State University College of Medicine, Department of Pediatrics, Columbus, OH, USA.<br /><searchLink fieldCode="AU" term="%22Mouhlas+D%22">Mouhlas D</searchLink>; The Institute for Genomic Medicine at Nationwide Children's Hospital, Columbus, OH, USA; The Ohio State University College of Medicine, Department of Pediatrics, Columbus, OH, USA.<br /><searchLink fieldCode="AU" term="%22Pyatt+R%22">Pyatt R</searchLink>; The Institute for Genomic Medicine at Nationwide Children's Hospital, Columbus, OH, USA; The Ohio State University College of Medicine, Department of Pathology, Columbus, OH, USA.<br /><searchLink fieldCode="AU" term="%22Reshmi+SC%22">Reshmi SC</searchLink>; The Institute for Genomic Medicine at Nationwide Children's Hospital, Columbus, OH, USA; The Ohio State University College of Medicine, Department of Pathology, Columbus, OH, USA.<br /><searchLink fieldCode="AU" term="%22Gastier-Foster+JM%22">Gastier-Foster JM</searchLink>; The Institute for Genomic Medicine at Nationwide Children's Hospital, Columbus, OH, USA; The Ohio State University College of Medicine, Department of Pediatrics, Columbus, OH, USA; The Ohio State University College of Medicine, Department of Pathology, Columbus, OH, USA.<br /><searchLink fieldCode="AU" term="%22Pfau+R%22">Pfau R</searchLink>; The Institute for Genomic Medicine at Nationwide Children's Hospital, Columbus, OH, USA; The Ohio State University College of Medicine, Department of Pathology, Columbus, OH, USA.<br /><searchLink fieldCode="AU" term="%22Astbury+C%22">Astbury C</searchLink>; The Institute for Genomic Medicine at Nationwide Children's Hospital, Columbus, OH, USA; The Ohio State University College of Medicine, Department of Pathology, Columbus, OH, USA. Electronic address: astburc@ccf.org. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22101247089%22">European journal of medical genetics</searchLink> [Eur J Med Genet] 2018 Jul; Vol. 61 (7), pp. 416-420. <i>Date of Electronic Publication: </i>2018 Mar 20. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Elsevier%22">Elsevier </searchLink><i>Country of Publication: </i>Netherlands <i>NLM ID: </i>101247089 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1878-0849 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2217697212%22">17697212 </searchLink><i>NLM ISO Abbreviation: </i>Eur J Med Genet <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=29572065 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1016/j.ejmg.2018.02.008 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 416 Titles: – TitleFull: Pericentromeric regions of homozygosity on the X chromosome: Another likely benign population variant. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Barrie ES – PersonEntity: Name: NameFull: Li Y – PersonEntity: Name: NameFull: Lamb-Thrush D – PersonEntity: Name: NameFull: Hashimoto S – PersonEntity: Name: NameFull: Matthews T – PersonEntity: Name: NameFull: Mouhlas D – PersonEntity: Name: NameFull: Pyatt R – PersonEntity: Name: NameFull: Reshmi SC – PersonEntity: Name: NameFull: Gastier-Foster JM – PersonEntity: Name: NameFull: Pfau R – PersonEntity: Name: NameFull: Astbury C IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 07 Text: 2018 Jul Type: published Y: 2018 Identifiers: – Type: issn-electronic Value: 1878-0849 Numbering: – Type: volume Value: 61 – Type: issue Value: 7 Titles: – TitleFull: European journal of medical genetics Type: main |
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