Homozygosity mapping identifies genetic defects in four consanguineous families with retinal dystrophy from Pakistan.
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| Title: | Homozygosity mapping identifies genetic defects in four consanguineous families with retinal dystrophy from Pakistan. |
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| Authors: | Khan, MI1,2, Ajmal, M1,2,3, Micheal, S1,2,4, Azam, M1,2, Hussain, A1, Shahzad, A3, Venselaar, H5, Bokhari, H1, de Wijs, IJ2, Hoefsloot, LH2, Waheed, NK6, Collin, RWJ2,7, den Hollander, AI2,4,7, Qamar, R1,3, Cremers, FPM1,2,7 |
| Source: | Clinical Genetics. Sep2013, Vol. 84 Issue 3, p290-293. 4p. 1 Diagram, 2 Charts, 1 Graph. |
| Database: | Academic Search Ultimate |
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| Header | DbId: asn DbLabel: Academic Search Ultimate An: 89680241 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=89680241 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1111/cge.12039 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 4 StartPage: 290 Titles: – TitleFull: Homozygosity mapping identifies genetic defects in four consanguineous families with retinal dystrophy from Pakistan. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Khan, MI – PersonEntity: Name: NameFull: Ajmal, M – PersonEntity: Name: NameFull: Micheal, S – PersonEntity: Name: NameFull: Azam, M – PersonEntity: Name: NameFull: Hussain, A – PersonEntity: Name: NameFull: Shahzad, A – PersonEntity: Name: NameFull: Venselaar, H – PersonEntity: Name: NameFull: Bokhari, H – PersonEntity: Name: NameFull: de Wijs, IJ – PersonEntity: Name: NameFull: Hoefsloot, LH – PersonEntity: Name: NameFull: Waheed, NK – PersonEntity: Name: NameFull: Collin, RWJ – PersonEntity: Name: NameFull: den Hollander, AI – PersonEntity: Name: NameFull: Qamar, R – PersonEntity: Name: NameFull: Cremers, FPM IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 09 Text: Sep2013 Type: published Y: 2013 Identifiers: – Type: issn-print Value: 00099163 Numbering: – Type: volume Value: 84 – Type: issue Value: 3 Titles: – TitleFull: Clinical Genetics Type: main |
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