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Clinical report follow up: Type 1 Collagenopathy presenting with a Russell-Silver phenotype.

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Title: Clinical report follow up: Type 1 Collagenopathy presenting with a Russell-Silver phenotype.
Authors: Kanani F; Sheffield Clinical Genetics Service, Sheffield Children's NHS Foundation Trust, Sheffield, United Kingdom., Parker MJ; Sheffield Clinical Genetics Service, Sheffield Children's NHS Foundation Trust, Sheffield, United Kingdom., Burren CP; University Hospitals Bristol NHS Foundation Trust, Bristol, United Kingdom., Rankin J; Royal Devon and Exeter NHS Trust, Exeter, United Kingdom., Balasubramanian M; Sheffield Clinical Genetics Service, Sheffield Children's NHS Foundation Trust, Sheffield, United Kingdom.
Source: American journal of medical genetics. Part A [Am J Med Genet A] 2019 Jan; Vol. 179 (1), pp. 139-140. Date of Electronic Publication: 2018 Dec 17.
Publication Type: Letter; Comment
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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PubType: Editorial & Opinion
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  Data: Clinical report follow up: Type 1 Collagenopathy presenting with a Russell-Silver phenotype.
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  Data: <searchLink fieldCode="AU" term="%22Kanani+F%22">Kanani F</searchLink>; Sheffield Clinical Genetics Service, Sheffield Children's NHS Foundation Trust, Sheffield, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Parker+MJ%22">Parker MJ</searchLink>; Sheffield Clinical Genetics Service, Sheffield Children's NHS Foundation Trust, Sheffield, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Burren+CP%22">Burren CP</searchLink>; University Hospitals Bristol NHS Foundation Trust, Bristol, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Rankin+J%22">Rankin J</searchLink>; Royal Devon and Exeter NHS Trust, Exeter, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Balasubramanian+M%22">Balasubramanian M</searchLink>; Sheffield Clinical Genetics Service, Sheffield Children's NHS Foundation Trust, Sheffield, United Kingdom.
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  Data: <searchLink fieldCode="JN" term="%22101235741%22">American journal of medical genetics. Part A</searchLink> [Am J Med Genet A] 2019 Jan; Vol. 179 (1), pp. 139-140. <i>Date of Electronic Publication: </i>2018 Dec 17.
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  Data: Letter; Comment
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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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        Value: 10.1002/ajmg.a.60680
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      – Code: eng
        Text: English
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        StartPage: 139
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      – TitleFull: Clinical report follow up: Type 1 Collagenopathy presenting with a Russell-Silver phenotype.
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            NameFull: Kanani F
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              Text: 2019 Jan
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              Value: 179
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            – TitleFull: American journal of medical genetics. Part A
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