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Whole-Exome sequencing identifies FAM20A mutations as a cause of amelogenesis imperfecta and gingival hyperplasia syndrome.

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Title: Whole-Exome sequencing identifies FAM20A mutations as a cause of amelogenesis imperfecta and gingival hyperplasia syndrome.
Authors: O'Sullivan J; Faculty of Medical and Human Sciences, Manchester Academic Health Sciences Centre, University of Manchester, Oxford Road, Manchester, UK., Bitu CC, Daly SB, Urquhart JE, Barron MJ, Bhaskar SS, Martelli-Júnior H, dos Santos Neto PE, Mansilla MA, Murray JC, Coletta RD, Black GC, Dixon MJ
Source: American journal of human genetics [Am J Hum Genet] 2011 May 13; Vol. 88 (5), pp. 616-20. Date of Electronic Publication: 2011 May 05.
Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Cell Press Country of Publication: United States NLM ID: 0370475 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1537-6605 (Electronic) Linking ISSN: 00029297 NLM ISO Abbreviation: Am J Hum Genet Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Whole-Exome sequencing identifies FAM20A mutations as a cause of amelogenesis imperfecta and gingival hyperplasia syndrome.
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  Data: <searchLink fieldCode="AU" term="%22O'Sullivan+J%22">O'Sullivan J</searchLink>; Faculty of Medical and Human Sciences, Manchester Academic Health Sciences Centre, University of Manchester, Oxford Road, Manchester, UK.<br /><searchLink fieldCode="AU" term="%22Bitu+CC%22">Bitu CC</searchLink><br /><searchLink fieldCode="AU" term="%22Daly+SB%22">Daly SB</searchLink><br /><searchLink fieldCode="AU" term="%22Urquhart+JE%22">Urquhart JE</searchLink><br /><searchLink fieldCode="AU" term="%22Barron+MJ%22">Barron MJ</searchLink><br /><searchLink fieldCode="AU" term="%22Bhaskar+SS%22">Bhaskar SS</searchLink><br /><searchLink fieldCode="AU" term="%22Martelli-Júnior+H%22">Martelli-Júnior H</searchLink><br /><searchLink fieldCode="AU" term="%22dos+Santos+Neto+PE%22">dos Santos Neto PE</searchLink><br /><searchLink fieldCode="AU" term="%22Mansilla+MA%22">Mansilla MA</searchLink><br /><searchLink fieldCode="AU" term="%22Murray+JC%22">Murray JC</searchLink><br /><searchLink fieldCode="AU" term="%22Coletta+RD%22">Coletta RD</searchLink><br /><searchLink fieldCode="AU" term="%22Black+GC%22">Black GC</searchLink><br /><searchLink fieldCode="AU" term="%22Dixon+MJ%22">Dixon MJ</searchLink>
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  Data: <searchLink fieldCode="JN" term="%220370475%22">American journal of human genetics</searchLink> [Am J Hum Genet] 2011 May 13; Vol. 88 (5), pp. 616-20. <i>Date of Electronic Publication: </i>2011 May 05.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Cell+Press%22">Cell Press </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>0370475 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1537-6605 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2200029297%22">00029297 </searchLink><i>NLM ISO Abbreviation: </i>Am J Hum Genet <i>Subsets: </i>MEDLINE
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        Value: 10.1016/j.ajhg.2011.04.005
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