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Point mutation frequency in the FMR1 gene as revealed by fragile X syndrome screening.

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Title: Point mutation frequency in the FMR1 gene as revealed by fragile X syndrome screening.
Authors: Handt M; Faculty of Health, Witten/Herdecke University, Alfred-Herrhausen-Straße 50, 58448 Witten, Germany., Epplen A; Human Genetics, Ruhr-University, Universitätsstraße 150, 44801 Bochum, Germany., Hoffjan S; Human Genetics, Ruhr-University, Universitätsstraße 150, 44801 Bochum, Germany., Mese K; Faculty of Health, Witten/Herdecke University, Alfred-Herrhausen-Straße 50, 58448 Witten, Germany., Epplen JT; Faculty of Health, Witten/Herdecke University, Alfred-Herrhausen-Straße 50, 58448 Witten, Germany; Human Genetics, Ruhr-University, Universitätsstraße 150, 44801 Bochum, Germany., Dekomien G; Human Genetics, Ruhr-University, Universitätsstraße 150, 44801 Bochum, Germany. Electronic address: gabriele.dekomien@rub.de.
Source: Molecular and cellular probes [Mol Cell Probes] 2014 Oct-Dec; Vol. 28 (5-6), pp. 279-83. Date of Electronic Publication: 2014 Aug 27.
Publication Type: Journal Article
Journal Info: Publisher: Academic Press Country of Publication: England NLM ID: 8709751 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1096-1194 (Electronic) Linking ISSN: 08908508 NLM ISO Abbreviation: Mol Cell Probes Subsets: MEDLINE
Database: MEDLINE Ultimate
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PubType: Academic Journal
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  Data: Point mutation frequency in the FMR1 gene as revealed by fragile X syndrome screening.
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  Data: <searchLink fieldCode="AU" term="%22Handt+M%22">Handt M</searchLink>; Faculty of Health, Witten/Herdecke University, Alfred-Herrhausen-Straße 50, 58448 Witten, Germany.<br /><searchLink fieldCode="AU" term="%22Epplen+A%22">Epplen A</searchLink>; Human Genetics, Ruhr-University, Universitätsstraße 150, 44801 Bochum, Germany.<br /><searchLink fieldCode="AU" term="%22Hoffjan+S%22">Hoffjan S</searchLink>; Human Genetics, Ruhr-University, Universitätsstraße 150, 44801 Bochum, Germany.<br /><searchLink fieldCode="AU" term="%22Mese+K%22">Mese K</searchLink>; Faculty of Health, Witten/Herdecke University, Alfred-Herrhausen-Straße 50, 58448 Witten, Germany.<br /><searchLink fieldCode="AU" term="%22Epplen+JT%22">Epplen JT</searchLink>; Faculty of Health, Witten/Herdecke University, Alfred-Herrhausen-Straße 50, 58448 Witten, Germany; Human Genetics, Ruhr-University, Universitätsstraße 150, 44801 Bochum, Germany.<br /><searchLink fieldCode="AU" term="%22Dekomien+G%22">Dekomien G</searchLink>; Human Genetics, Ruhr-University, Universitätsstraße 150, 44801 Bochum, Germany. Electronic address: gabriele.dekomien@rub.de.
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  Data: <searchLink fieldCode="JN" term="%228709751%22">Molecular and cellular probes</searchLink> [Mol Cell Probes] 2014 Oct-Dec; Vol. 28 (5-6), pp. 279-83. <i>Date of Electronic Publication: </i>2014 Aug 27.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Academic+Press%22">Academic Press </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>8709751 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1096-1194 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2208908508%22">08908508 </searchLink><i>NLM ISO Abbreviation: </i>Mol Cell Probes <i>Subsets: </i>MEDLINE
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      – Type: doi
        Value: 10.1016/j.mcp.2014.08.003
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      – Code: eng
        Text: English
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      – TitleFull: Point mutation frequency in the FMR1 gene as revealed by fragile X syndrome screening.
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            NameFull: Handt M
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            NameFull: Epplen A
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              Text: 2014 Oct-Dec
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              Value: 28
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              Value: 5-6
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            – TitleFull: Molecular and cellular probes
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