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Exome sequencing identifies mutations in the gene TTC7A in French-Canadian cases with hereditary multiple intestinal atresia.

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Title: Exome sequencing identifies mutations in the gene TTC7A in French-Canadian cases with hereditary multiple intestinal atresia.
Authors: Samuels ME; Centre de Recherche du CHU Ste-Justine, University of Montreal, Montreal, Quebec, Canada, Majewski J, Alirezaie N, Fernandez I, Casals F, Patey N, Decaluwe H, Gosselin I, Haddad E, Hodgkinson A, Idaghdour Y, Marchand V, Michaud JL, Rodrigue MA, Desjardins S, Dubois S, Le Deist F, Awadalla P, Raymond V, Maranda B
Source: Journal of medical genetics [J Med Genet] 2013 May; Vol. 50 (5), pp. 324-9. Date of Electronic Publication: 2013 Feb 19.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: British Medical Association Country of Publication: England NLM ID: 2985087R Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1468-6244 (Electronic) Linking ISSN: 00222593 NLM ISO Abbreviation: J Med Genet Subsets: MEDLINE
Database: MEDLINE Ultimate
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PubType: Academic Journal
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  Data: Exome sequencing identifies mutations in the gene TTC7A in French-Canadian cases with hereditary multiple intestinal atresia.
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  Data: <searchLink fieldCode="AU" term="%22Samuels+ME%22">Samuels ME</searchLink>; Centre de Recherche du CHU Ste-Justine, University of Montreal, Montreal, Quebec, Canada<br /><searchLink fieldCode="AU" term="%22Majewski+J%22">Majewski J</searchLink><br /><searchLink fieldCode="AU" term="%22Alirezaie+N%22">Alirezaie N</searchLink><br /><searchLink fieldCode="AU" term="%22Fernandez+I%22">Fernandez I</searchLink><br /><searchLink fieldCode="AU" term="%22Casals+F%22">Casals F</searchLink><br /><searchLink fieldCode="AU" term="%22Patey+N%22">Patey N</searchLink><br /><searchLink fieldCode="AU" term="%22Decaluwe+H%22">Decaluwe H</searchLink><br /><searchLink fieldCode="AU" term="%22Gosselin+I%22">Gosselin I</searchLink><br /><searchLink fieldCode="AU" term="%22Haddad+E%22">Haddad E</searchLink><br /><searchLink fieldCode="AU" term="%22Hodgkinson+A%22">Hodgkinson A</searchLink><br /><searchLink fieldCode="AU" term="%22Idaghdour+Y%22">Idaghdour Y</searchLink><br /><searchLink fieldCode="AU" term="%22Marchand+V%22">Marchand V</searchLink><br /><searchLink fieldCode="AU" term="%22Michaud+JL%22">Michaud JL</searchLink><br /><searchLink fieldCode="AU" term="%22Rodrigue+MA%22">Rodrigue MA</searchLink><br /><searchLink fieldCode="AU" term="%22Desjardins+S%22">Desjardins S</searchLink><br /><searchLink fieldCode="AU" term="%22Dubois+S%22">Dubois S</searchLink><br /><searchLink fieldCode="AU" term="%22Le+Deist+F%22">Le Deist F</searchLink><br /><searchLink fieldCode="AU" term="%22Awadalla+P%22">Awadalla P</searchLink><br /><searchLink fieldCode="AU" term="%22Raymond+V%22">Raymond V</searchLink><br /><searchLink fieldCode="AU" term="%22Maranda+B%22">Maranda B</searchLink>
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  Data: <searchLink fieldCode="JN" term="%222985087R%22">Journal of medical genetics</searchLink> [J Med Genet] 2013 May; Vol. 50 (5), pp. 324-9. <i>Date of Electronic Publication: </i>2013 Feb 19.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22British+Medical+Association%22">British Medical Association </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>2985087R <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1468-6244 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2200222593%22">00222593 </searchLink><i>NLM ISO Abbreviation: </i>J Med Genet <i>Subsets: </i>MEDLINE
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=23423984
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        Value: 10.1136/jmedgenet-2012-101483
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      – Code: eng
        Text: English
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              Text: 2013 May
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