Genome-wide scans of myopia in Pennsylvania Amish families reveal significant linkage to 12q15, 8q21.3 and 5p15.33.
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| Title: | Genome-wide scans of myopia in Pennsylvania Amish families reveal significant linkage to 12q15, 8q21.3 and 5p15.33. |
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| Authors: | Musolf AM; Computational and Statistical Genomics Branch, National Human Genome Research Institute, National Institutes of Health, 333 Cassell Dr, Suite 1200, Baltimore, MD, 21224, USA., Simpson CL; Computational and Statistical Genomics Branch, National Human Genome Research Institute, National Institutes of Health, 333 Cassell Dr, Suite 1200, Baltimore, MD, 21224, USA.; Department of Genetics, Genomics and Informatics, University of Tennessee Health Science Center, Memphis, TN, USA.; Department of Ophthalmology, University of Tennessee Health Science Center, Memphis, TN, USA., Alexander TA; Computational and Statistical Genomics Branch, National Human Genome Research Institute, National Institutes of Health, 333 Cassell Dr, Suite 1200, Baltimore, MD, 21224, USA., Portas L; Computational and Statistical Genomics Branch, National Human Genome Research Institute, National Institutes of Health, 333 Cassell Dr, Suite 1200, Baltimore, MD, 21224, USA., Murgia F; Computational and Statistical Genomics Branch, National Human Genome Research Institute, National Institutes of Health, 333 Cassell Dr, Suite 1200, Baltimore, MD, 21224, USA., Ciner EB; The Pennsylvania College of Optometry at Salus University, Elkins Park, PA, USA., Stambolian D; Department of Ophthalmology, University of Pennsylvania, Philadelphia, PA, USA., Bailey-Wilson JE; Computational and Statistical Genomics Branch, National Human Genome Research Institute, National Institutes of Health, 333 Cassell Dr, Suite 1200, Baltimore, MD, 21224, USA. jebw@mail.nih.gov. |
| Source: | Human genetics [Hum Genet] 2019 Apr; Vol. 138 (4), pp. 339-354. Date of Electronic Publication: 2019 Mar 02. |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: Springer Verlag Country of Publication: Germany NLM ID: 7613873 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1432-1203 (Electronic) Linking ISSN: 03406717 NLM ISO Abbreviation: Hum Genet Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 30826882 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Genome-wide scans of myopia in Pennsylvania Amish families reveal significant linkage to 12q15, 8q21.3 and 5p15.33. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Musolf+AM%22">Musolf AM</searchLink>; Computational and Statistical Genomics Branch, National Human Genome Research Institute, National Institutes of Health, 333 Cassell Dr, Suite 1200, Baltimore, MD, 21224, USA.<br /><searchLink fieldCode="AU" term="%22Simpson+CL%22">Simpson CL</searchLink>; Computational and Statistical Genomics Branch, National Human Genome Research Institute, National Institutes of Health, 333 Cassell Dr, Suite 1200, Baltimore, MD, 21224, USA.; Department of Genetics, Genomics and Informatics, University of Tennessee Health Science Center, Memphis, TN, USA.; Department of Ophthalmology, University of Tennessee Health Science Center, Memphis, TN, USA.<br /><searchLink fieldCode="AU" term="%22Alexander+TA%22">Alexander TA</searchLink>; Computational and Statistical Genomics Branch, National Human Genome Research Institute, National Institutes of Health, 333 Cassell Dr, Suite 1200, Baltimore, MD, 21224, USA.<br /><searchLink fieldCode="AU" term="%22Portas+L%22">Portas L</searchLink>; Computational and Statistical Genomics Branch, National Human Genome Research Institute, National Institutes of Health, 333 Cassell Dr, Suite 1200, Baltimore, MD, 21224, USA.<br /><searchLink fieldCode="AU" term="%22Murgia+F%22">Murgia F</searchLink>; Computational and Statistical Genomics Branch, National Human Genome Research Institute, National Institutes of Health, 333 Cassell Dr, Suite 1200, Baltimore, MD, 21224, USA.<br /><searchLink fieldCode="AU" term="%22Ciner+EB%22">Ciner EB</searchLink>; The Pennsylvania College of Optometry at Salus University, Elkins Park, PA, USA.<br /><searchLink fieldCode="AU" term="%22Stambolian+D%22">Stambolian D</searchLink>; Department of Ophthalmology, University of Pennsylvania, Philadelphia, PA, USA.<br /><searchLink fieldCode="AU" term="%22Bailey-Wilson+JE%22">Bailey-Wilson JE</searchLink>; Computational and Statistical Genomics Branch, National Human Genome Research Institute, National Institutes of Health, 333 Cassell Dr, Suite 1200, Baltimore, MD, 21224, USA. jebw@mail.nih.gov. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%227613873%22">Human genetics</searchLink> [Hum Genet] 2019 Apr; Vol. 138 (4), pp. 339-354. <i>Date of Electronic Publication: </i>2019 Mar 02. – 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="%22Springer+Verlag%22">Springer Verlag </searchLink><i>Country of Publication: </i>Germany <i>NLM ID: </i>7613873 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1432-1203 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2203406717%22">03406717 </searchLink><i>NLM ISO Abbreviation: </i>Hum Genet <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=30826882 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1007/s00439-019-01991-0 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 339 Titles: – TitleFull: Genome-wide scans of myopia in Pennsylvania Amish families reveal significant linkage to 12q15, 8q21.3 and 5p15.33. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Musolf AM – PersonEntity: Name: NameFull: Simpson CL – PersonEntity: Name: NameFull: Alexander TA – PersonEntity: Name: NameFull: Portas L – PersonEntity: Name: NameFull: Murgia F – PersonEntity: Name: NameFull: Ciner EB – PersonEntity: Name: NameFull: Stambolian D – PersonEntity: Name: NameFull: Bailey-Wilson JE IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 04 Text: 2019 Apr Type: published Y: 2019 Identifiers: – Type: issn-electronic Value: 1432-1203 Numbering: – Type: volume Value: 138 – Type: issue Value: 4 Titles: – TitleFull: Human genetics Type: main |
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