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Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHE.

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Title: Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHE.
Authors: Celestino-Soper PB; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA., Shaw CA, Sanders SJ, Li J, Murtha MT, Ercan-Sencicek AG, Davis L, Thomson S, Gambin T, Chinault AC, Ou Z, German JR, Milosavljevic A, Sutcliffe JS, Cook EH Jr, Stankiewicz P, State MW, Beaudet AL
Source: Human molecular genetics [Hum Mol Genet] 2011 Nov 15; Vol. 20 (22), pp. 4360-70. Date of Electronic Publication: 2011 Aug 24.
Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
Journal Info: Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1460-2083 (Electronic) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHE.
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  Data: <searchLink fieldCode="AU" term="%22Celestino-Soper+PB%22">Celestino-Soper PB</searchLink>; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.<br /><searchLink fieldCode="AU" term="%22Shaw+CA%22">Shaw CA</searchLink><br /><searchLink fieldCode="AU" term="%22Sanders+SJ%22">Sanders SJ</searchLink><br /><searchLink fieldCode="AU" term="%22Li+J%22">Li J</searchLink><br /><searchLink fieldCode="AU" term="%22Murtha+MT%22">Murtha MT</searchLink><br /><searchLink fieldCode="AU" term="%22Ercan-Sencicek+AG%22">Ercan-Sencicek AG</searchLink><br /><searchLink fieldCode="AU" term="%22Davis+L%22">Davis L</searchLink><br /><searchLink fieldCode="AU" term="%22Thomson+S%22">Thomson S</searchLink><br /><searchLink fieldCode="AU" term="%22Gambin+T%22">Gambin T</searchLink><br /><searchLink fieldCode="AU" term="%22Chinault+AC%22">Chinault AC</searchLink><br /><searchLink fieldCode="AU" term="%22Ou+Z%22">Ou Z</searchLink><br /><searchLink fieldCode="AU" term="%22German+JR%22">German JR</searchLink><br /><searchLink fieldCode="AU" term="%22Milosavljevic+A%22">Milosavljevic A</searchLink><br /><searchLink fieldCode="AU" term="%22Sutcliffe+JS%22">Sutcliffe JS</searchLink><br /><searchLink fieldCode="AU" term="%22Cook+EH+Jr%22">Cook EH Jr</searchLink><br /><searchLink fieldCode="AU" term="%22Stankiewicz+P%22">Stankiewicz P</searchLink><br /><searchLink fieldCode="AU" term="%22State+MW%22">State MW</searchLink><br /><searchLink fieldCode="AU" term="%22Beaudet+AL%22">Beaudet AL</searchLink>
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  Data: <searchLink fieldCode="JN" term="%229208958%22">Human molecular genetics</searchLink> [Hum Mol Genet] 2011 Nov 15; Vol. 20 (22), pp. 4360-70. <i>Date of Electronic Publication: </i>2011 Aug 24.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22IRL+Press+at+Oxford+University+Press%22">IRL Press at Oxford University Press </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>9208958 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1460-2083 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2209646906%22">09646906 </searchLink><i>NLM ISO Abbreviation: </i>Hum Mol Genet <i>Subsets: </i>MEDLINE
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        Value: 10.1093/hmg/ddr363
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              Text: 2011 Nov 15
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