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Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene.

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Title: Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene.
Authors: Dietz HC; Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205., Cutting GR, Pyeritz RE, Maslen CL, Sakai LY, Corson GM, Puffenberger EG, Hamosh A, Nanthakumar EJ, Curristin SM, et. al.
Source: Nature [Nature] 1991 Jul 25; Vol. 352 (6333), pp. 337-9.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
Journal Info: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 0410462 Publication Model: Print Cited Medium: Print ISSN: 0028-0836 (Print) Linking ISSN: 00280836 NLM ISO Abbreviation: Nature Subsets: MEDLINE
Database: MEDLINE Ultimate
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PubType: Academic Journal
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  Data: Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene.
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  Data: <searchLink fieldCode="AU" term="%22Dietz+HC%22">Dietz HC</searchLink>; Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.<br /><searchLink fieldCode="AU" term="%22Cutting+GR%22">Cutting GR</searchLink><br /><searchLink fieldCode="AU" term="%22Pyeritz+RE%22">Pyeritz RE</searchLink><br /><searchLink fieldCode="AU" term="%22Maslen+CL%22">Maslen CL</searchLink><br /><searchLink fieldCode="AU" term="%22Sakai+LY%22">Sakai LY</searchLink><br /><searchLink fieldCode="AU" term="%22Corson+GM%22">Corson GM</searchLink><br /><searchLink fieldCode="AU" term="%22Puffenberger+EG%22">Puffenberger EG</searchLink><br /><searchLink fieldCode="AU" term="%22Hamosh+A%22">Hamosh A</searchLink><br /><searchLink fieldCode="AU" term="%22Nanthakumar+EJ%22">Nanthakumar EJ</searchLink><br /><searchLink fieldCode="AU" term="%22Curristin+SM%22">Curristin SM</searchLink><br />et. al.
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  Data: <searchLink fieldCode="JN" term="%220410462%22">Nature</searchLink> [Nature] 1991 Jul 25; Vol. 352 (6333), pp. 337-9.
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  Data: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Nature+Publishing+Group%22">Nature Publishing Group </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>0410462 <i>Publication Model: </i>Print <i>Cited Medium: </i>Print <i>ISSN: </i>0028-0836 (Print) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2200280836%22">00280836 </searchLink><i>NLM ISO Abbreviation: </i>Nature <i>Subsets: </i>MEDLINE
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      – Type: doi
        Value: 10.1038/352337a0
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      – Code: eng
        Text: English
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        StartPage: 337
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      – TitleFull: Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene.
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            NameFull: Dietz HC
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            NameFull: Cutting GR
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            NameFull: Pyeritz RE
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            – D: 25
              M: 07
              Text: 1991 Jul 25
              Type: published
              Y: 1991
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              Value: 0028-0836
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              Value: 352
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              Value: 6333
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            – TitleFull: Nature
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