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Family with congenital contractural arachnodactyly due to a novel multiexon deletion of the FBN2 gene.

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Title: Family with congenital contractural arachnodactyly due to a novel multiexon deletion of the FBN2 gene.
Authors: Yagi H; Department of Cardiovascular Medicine The University of Tokyo Hospital Tokyo Japan.; Marfan Syndrome Center The University of Tokyo Hospital Tokyo Japan., Takiguchi H; Department of Cardiovascular Medicine The University of Tokyo Hospital Tokyo Japan., Takeda N; Department of Cardiovascular Medicine The University of Tokyo Hospital Tokyo Japan.; Marfan Syndrome Center The University of Tokyo Hospital Tokyo Japan., Inuzuka R; Marfan Syndrome Center The University of Tokyo Hospital Tokyo Japan.; Department of Pediatrics The University of Tokyo Hospital Tokyo Japan., Taniguchi Y; Marfan Syndrome Center The University of Tokyo Hospital Tokyo Japan.; Department of Orthopedic Surgery The University of Tokyo Hospital Tokyo Japan., Porto KJ; Department of Neurology The University of Tokyo Hospital Tokyo Japan., Ishiura H; Department of Neurology The University of Tokyo Hospital Tokyo Japan., Mitsui J; Department of Neurology The University of Tokyo Hospital Tokyo Japan., Morita H; Department of Cardiovascular Medicine The University of Tokyo Hospital Tokyo Japan., Komuro I; Department of Cardiovascular Medicine The University of Tokyo Hospital Tokyo Japan.
Source: Clinical case reports [Clin Case Rep] 2022 Feb 09; Vol. 10 (2), pp. e05335. Date of Electronic Publication: 2022 Feb 09 (Print Publication: 2022).
Publication Type: Case Reports; Journal Article
Journal Info: Publisher: John Wiley & Sons Country of Publication: England NLM ID: 101620385 Publication Model: eCollection Cited Medium: Print ISSN: 2050-0904 (Print) Linking ISSN: 20500904 NLM ISO Abbreviation: Clin Case Rep Subsets: PubMed not MEDLINE
Database: MEDLINE Ultimate
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  Data: Family with congenital contractural arachnodactyly due to a novel multiexon deletion of the FBN2 gene.
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  Data: <searchLink fieldCode="AU" term="%22Yagi+H%22">Yagi H</searchLink>; Department of Cardiovascular Medicine The University of Tokyo Hospital Tokyo Japan.; Marfan Syndrome Center The University of Tokyo Hospital Tokyo Japan.<br /><searchLink fieldCode="AU" term="%22Takiguchi+H%22">Takiguchi H</searchLink>; Department of Cardiovascular Medicine The University of Tokyo Hospital Tokyo Japan.<br /><searchLink fieldCode="AU" term="%22Takeda+N%22">Takeda N</searchLink>; Department of Cardiovascular Medicine The University of Tokyo Hospital Tokyo Japan.; Marfan Syndrome Center The University of Tokyo Hospital Tokyo Japan.<br /><searchLink fieldCode="AU" term="%22Inuzuka+R%22">Inuzuka R</searchLink>; Marfan Syndrome Center The University of Tokyo Hospital Tokyo Japan.; Department of Pediatrics The University of Tokyo Hospital Tokyo Japan.<br /><searchLink fieldCode="AU" term="%22Taniguchi+Y%22">Taniguchi Y</searchLink>; Marfan Syndrome Center The University of Tokyo Hospital Tokyo Japan.; Department of Orthopedic Surgery The University of Tokyo Hospital Tokyo Japan.<br /><searchLink fieldCode="AU" term="%22Porto+KJ%22">Porto KJ</searchLink>; Department of Neurology The University of Tokyo Hospital Tokyo Japan.<br /><searchLink fieldCode="AU" term="%22Ishiura+H%22">Ishiura H</searchLink>; Department of Neurology The University of Tokyo Hospital Tokyo Japan.<br /><searchLink fieldCode="AU" term="%22Mitsui+J%22">Mitsui J</searchLink>; Department of Neurology The University of Tokyo Hospital Tokyo Japan.<br /><searchLink fieldCode="AU" term="%22Morita+H%22">Morita H</searchLink>; Department of Cardiovascular Medicine The University of Tokyo Hospital Tokyo Japan.<br /><searchLink fieldCode="AU" term="%22Komuro+I%22">Komuro I</searchLink>; Department of Cardiovascular Medicine The University of Tokyo Hospital Tokyo Japan.
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  Data: <searchLink fieldCode="JN" term="%22101620385%22">Clinical case reports</searchLink> [Clin Case Rep] 2022 Feb 09; Vol. 10 (2), pp. e05335. <i>Date of Electronic Publication: </i>2022 Feb 09 (<i>Print Publication: </i>2022).
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22John+Wiley+%26+Sons%22">John Wiley & Sons </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>101620385 <i>Publication Model: </i>eCollection <i>Cited Medium: </i>Print <i>ISSN: </i>2050-0904 (Print) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2220500904%22">20500904 </searchLink><i>NLM ISO Abbreviation: </i>Clin Case Rep <i>Subsets: </i>PubMed not MEDLINE
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        Value: 10.1002/ccr3.5335
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      – Code: eng
        Text: English
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        StartPage: e05335
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      – TitleFull: Family with congenital contractural arachnodactyly due to a novel multiexon deletion of the FBN2 gene.
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            NameFull: Yagi H
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            NameFull: Takiguchi H
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            NameFull: Ishiura H
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          Dates:
            – D: 09
              M: 02
              Text: 2022 Feb 09
              Type: published
              Y: 2022
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              Value: 2050-0904
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