Altered cerebrospinal fluid proteins in Smith-Lemli-Opitz syndrome patients.
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| Title: | Altered cerebrospinal fluid proteins in Smith-Lemli-Opitz syndrome patients. |
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| Authors: | Cologna SM; Section on Molecular Dysmorphology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Department of Health and Human Services, Bethesda, MD, USA.; Current Location: Department of Chemistry, University of Illinois at Chicago, Chicago, IL, USA., Shieh C; Section on Molecular Dysmorphology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Department of Health and Human Services, Bethesda, MD, USA., Toth CL; Section on Molecular Dysmorphology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Department of Health and Human Services, Bethesda, MD, USA., Cougnoux A; Section on Molecular Dysmorphology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Department of Health and Human Services, Bethesda, MD, USA., Burkert KR; Section on Molecular Dysmorphology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Department of Health and Human Services, Bethesda, MD, USA., Bianconi SE; Section on Molecular Dysmorphology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Department of Health and Human Services, Bethesda, MD, USA., Wassif CA; Section on Molecular Dysmorphology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Department of Health and Human Services, Bethesda, MD, USA., Porter FD; Section on Molecular Dysmorphology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Department of Health and Human Services, Bethesda, MD, USA. |
| Source: | American journal of medical genetics. Part A [Am J Med Genet A] 2016 Aug; Vol. 170 (8), pp. 2060-2068. Date of Electronic Publication: 2016 May 05. |
| Publication Type: | Journal Article; Research Support, N.I.H., Intramural; 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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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 27148958 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Altered cerebrospinal fluid proteins in Smith-Lemli-Opitz syndrome patients. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Cologna+SM%22">Cologna SM</searchLink>; Section on Molecular Dysmorphology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Department of Health and Human Services, Bethesda, MD, USA.; Current Location: Department of Chemistry, University of Illinois at Chicago, Chicago, IL, USA.<br /><searchLink fieldCode="AU" term="%22Shieh+C%22">Shieh C</searchLink>; Section on Molecular Dysmorphology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Department of Health and Human Services, Bethesda, MD, USA.<br /><searchLink fieldCode="AU" term="%22Toth+CL%22">Toth CL</searchLink>; Section on Molecular Dysmorphology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Department of Health and Human Services, Bethesda, MD, USA.<br /><searchLink fieldCode="AU" term="%22Cougnoux+A%22">Cougnoux A</searchLink>; Section on Molecular Dysmorphology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Department of Health and Human Services, Bethesda, MD, USA.<br /><searchLink fieldCode="AU" term="%22Burkert+KR%22">Burkert KR</searchLink>; Section on Molecular Dysmorphology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Department of Health and Human Services, Bethesda, MD, USA.<br /><searchLink fieldCode="AU" term="%22Bianconi+SE%22">Bianconi SE</searchLink>; Section on Molecular Dysmorphology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Department of Health and Human Services, Bethesda, MD, USA.<br /><searchLink fieldCode="AU" term="%22Wassif+CA%22">Wassif CA</searchLink>; Section on Molecular Dysmorphology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Department of Health and Human Services, Bethesda, MD, USA.<br /><searchLink fieldCode="AU" term="%22Porter+FD%22">Porter FD</searchLink>; Section on Molecular Dysmorphology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Department of Health and Human Services, Bethesda, MD, USA. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22101235741%22">American journal of medical genetics. Part A</searchLink> [Am J Med Genet A] 2016 Aug; Vol. 170 (8), pp. 2060-2068. <i>Date of Electronic Publication: </i>2016 May 05. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article; Research Support, N.I.H., Intramural; Research Support, Non-U.S. Gov't – Name: TitleSource Label: Journal Info Group: Src 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 |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=27148958 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1002/ajmg.a.37720 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 2060 Titles: – TitleFull: Altered cerebrospinal fluid proteins in Smith-Lemli-Opitz syndrome patients. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Cologna SM – PersonEntity: Name: NameFull: Shieh C – PersonEntity: Name: NameFull: Toth CL – PersonEntity: Name: NameFull: Cougnoux A – PersonEntity: Name: NameFull: Burkert KR – PersonEntity: Name: NameFull: Bianconi SE – PersonEntity: Name: NameFull: Wassif CA – PersonEntity: Name: NameFull: Porter FD IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 08 Text: 2016 Aug Type: published Y: 2016 Identifiers: – Type: issn-electronic Value: 1552-4833 Numbering: – Type: volume Value: 170 – Type: issue Value: 8 Titles: – TitleFull: American journal of medical genetics. Part A Type: main |
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