X-linked isolated growth hormone deficiency: expanding the phenotypic spectrum of SOX3 polyalanine tract expansions.
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| Title: | X-linked isolated growth hormone deficiency: expanding the phenotypic spectrum of SOX3 polyalanine tract expansions. |
|---|---|
| Authors: | Burkitt Wright EM; University of Manchester and Central Manchester University Hospitals Foundation Trust, St Mary's Hospital, UK., Perveen R, Clayton PE, Hall CM, Costa T, Procter AM, Giblin CA, Donnai D, Black GC |
| Source: | Clinical dysmorphology [Clin Dysmorphol] 2009 Oct; Vol. 18 (4), pp. 218-21. |
| Publication Type: | Case Reports; Journal Article; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: Lippincott Williams & Wilkins Country of Publication: England NLM ID: 9207893 Publication Model: Print Cited Medium: Internet ISSN: 1473-5717 (Electronic) Linking ISSN: 09628827 NLM ISO Abbreviation: Clin Dysmorphol Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 19654509 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: X-linked isolated growth hormone deficiency: expanding the phenotypic spectrum of SOX3 polyalanine tract expansions. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Burkitt+Wright+EM%22">Burkitt Wright EM</searchLink>; University of Manchester and Central Manchester University Hospitals Foundation Trust, St Mary's Hospital, UK.<br /><searchLink fieldCode="AU" term="%22Perveen+R%22">Perveen R</searchLink><br /><searchLink fieldCode="AU" term="%22Clayton+PE%22">Clayton PE</searchLink><br /><searchLink fieldCode="AU" term="%22Hall+CM%22">Hall CM</searchLink><br /><searchLink fieldCode="AU" term="%22Costa+T%22">Costa T</searchLink><br /><searchLink fieldCode="AU" term="%22Procter+AM%22">Procter AM</searchLink><br /><searchLink fieldCode="AU" term="%22Giblin+CA%22">Giblin CA</searchLink><br /><searchLink fieldCode="AU" term="%22Donnai+D%22">Donnai D</searchLink><br /><searchLink fieldCode="AU" term="%22Black+GC%22">Black GC</searchLink> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%229207893%22">Clinical dysmorphology</searchLink> [Clin Dysmorphol] 2009 Oct; Vol. 18 (4), pp. 218-21. – Name: TypePub Label: Publication Type Group: TypPub Data: Case Reports; Journal Article; Research Support, Non-U.S. Gov't – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Lippincott+Williams+%26+Wilkins%22">Lippincott Williams & Wilkins </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>9207893 <i>Publication Model: </i>Print <i>Cited Medium: </i>Internet <i>ISSN: </i>1473-5717 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2209628827%22">09628827 </searchLink><i>NLM ISO Abbreviation: </i>Clin Dysmorphol <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=19654509 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1097/MCD.0b013e32832d06f0 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 218 Titles: – TitleFull: X-linked isolated growth hormone deficiency: expanding the phenotypic spectrum of SOX3 polyalanine tract expansions. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Burkitt Wright EM – PersonEntity: Name: NameFull: Perveen R – PersonEntity: Name: NameFull: Clayton PE – PersonEntity: Name: NameFull: Hall CM – PersonEntity: Name: NameFull: Costa T – PersonEntity: Name: NameFull: Procter AM – PersonEntity: Name: NameFull: Giblin CA – PersonEntity: Name: NameFull: Donnai D – PersonEntity: Name: NameFull: Black GC IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 10 Text: 2009 Oct Type: published Y: 2009 Identifiers: – Type: issn-electronic Value: 1473-5717 Numbering: – Type: volume Value: 18 – Type: issue Value: 4 Titles: – TitleFull: Clinical dysmorphology Type: main |
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