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Genotype-phenotype analysis of 4q deletion syndrome: proposal of a critical region.

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Title: Genotype-phenotype analysis of 4q deletion syndrome: proposal of a critical region.
Authors: Strehle EM; Institute of Human Genetics, Newcastle upon Tyne, United Kingdom., Yu L, Rosenfeld JA, Donkervoort S, Zhou Y, Chen TJ, Martinez JE, Fan YS, Barbouth D, Zhu H, Vaglio A, Smith R, Stevens CA, Curry CJ, Ladda RL, Fan ZJ, Fox JE, Martin JA, Abdel-Hamid HZ, McCracken EA, McGillivray BC, Masser-Frye D, Huang T
Source: American journal of medical genetics. Part A [Am J Med Genet A] 2012 Sep; Vol. 158A (9), pp. 2139-51. Date of Electronic Publication: 2012 Jul 27.
Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Genotype-phenotype analysis of 4q deletion syndrome: proposal of a critical region.
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  Data: <searchLink fieldCode="AU" term="%22Strehle+EM%22">Strehle EM</searchLink>; Institute of Human Genetics, Newcastle upon Tyne, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Yu+L%22">Yu L</searchLink><br /><searchLink fieldCode="AU" term="%22Rosenfeld+JA%22">Rosenfeld JA</searchLink><br /><searchLink fieldCode="AU" term="%22Donkervoort+S%22">Donkervoort S</searchLink><br /><searchLink fieldCode="AU" term="%22Zhou+Y%22">Zhou Y</searchLink><br /><searchLink fieldCode="AU" term="%22Chen+TJ%22">Chen TJ</searchLink><br /><searchLink fieldCode="AU" term="%22Martinez+JE%22">Martinez JE</searchLink><br /><searchLink fieldCode="AU" term="%22Fan+YS%22">Fan YS</searchLink><br /><searchLink fieldCode="AU" term="%22Barbouth+D%22">Barbouth D</searchLink><br /><searchLink fieldCode="AU" term="%22Zhu+H%22">Zhu H</searchLink><br /><searchLink fieldCode="AU" term="%22Vaglio+A%22">Vaglio A</searchLink><br /><searchLink fieldCode="AU" term="%22Smith+R%22">Smith R</searchLink><br /><searchLink fieldCode="AU" term="%22Stevens+CA%22">Stevens CA</searchLink><br /><searchLink fieldCode="AU" term="%22Curry+CJ%22">Curry CJ</searchLink><br /><searchLink fieldCode="AU" term="%22Ladda+RL%22">Ladda RL</searchLink><br /><searchLink fieldCode="AU" term="%22Fan+ZJ%22">Fan ZJ</searchLink><br /><searchLink fieldCode="AU" term="%22Fox+JE%22">Fox JE</searchLink><br /><searchLink fieldCode="AU" term="%22Martin+JA%22">Martin JA</searchLink><br /><searchLink fieldCode="AU" term="%22Abdel-Hamid+HZ%22">Abdel-Hamid HZ</searchLink><br /><searchLink fieldCode="AU" term="%22McCracken+EA%22">McCracken EA</searchLink><br /><searchLink fieldCode="AU" term="%22McGillivray+BC%22">McGillivray BC</searchLink><br /><searchLink fieldCode="AU" term="%22Masser-Frye+D%22">Masser-Frye D</searchLink><br /><searchLink fieldCode="AU" term="%22Huang+T%22">Huang T</searchLink>
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  Data: <searchLink fieldCode="JN" term="%22101235741%22">American journal of medical genetics. Part A</searchLink> [Am J Med Genet A] 2012 Sep; Vol. 158A (9), pp. 2139-51. <i>Date of Electronic Publication: </i>2012 Jul 27.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Wiley-Blackwell%22">Wiley-Blackwell </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>101235741 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1552-4833 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2215524825%22">15524825 </searchLink><i>NLM ISO Abbreviation: </i>Am J Med Genet A <i>Subsets: </i>MEDLINE
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