Neurodevelopmental delay, musculoskeletal disorders and dysmorphia associated with a novel pathogenic interstitial deletion of chromosome 10q21.1q21.3.
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| Title: | Neurodevelopmental delay, musculoskeletal disorders and dysmorphia associated with a novel pathogenic interstitial deletion of chromosome 10q21.1q21.3. |
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| Authors: | Dutta D; Division of Hematology/Oncology, Department of Medicine, SUNY Upstate Medical University, Syracuse, New York, USA duttad@upstate.edu gargri@upstate.edu., Black J; Center of Development, Behavior, and Genetics, SUNY Upstate Medical University, Syracuse, New York, USA., Montoya EA; Department of Pediatrics, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA., Burrow TA; Department of Pediatrics, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA., Shieh J; Division of Medical Genetics, Department of Pediatrics, University of California San Francisco, San Francisco, California, USA., McGivern B; GeneDx, Gaithersburg, Maryland, USA., Raymond M; GeneDx, Gaithersburg, Maryland, USA., Sheedy CB; GeneDx, Gaithersburg, Maryland, USA., Smith SC; Department of Pathology, SUNY Upstate Medical University, Syracuse, New York, USA., Garg R; Center of Development, Behavior, and Genetics, SUNY Upstate Medical University, Syracuse, New York, USA duttad@upstate.edu gargri@upstate.edu. |
| Source: | Journal of medical genetics [J Med Genet] 2025 Mar 20; Vol. 62 (4), pp. 268-275. Date of Electronic Publication: 2025 Mar 20. |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: British Medical Association Country of Publication: England NLM ID: 2985087R Publication Model: Electronic Cited Medium: Internet ISSN: 1468-6244 (Electronic) Linking ISSN: 00222593 NLM ISO Abbreviation: J Med Genet Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 39904608 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Neurodevelopmental delay, musculoskeletal disorders and dysmorphia associated with a novel pathogenic interstitial deletion of chromosome 10q21.1q21.3. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Dutta+D%22">Dutta D</searchLink>; Division of Hematology/Oncology, Department of Medicine, SUNY Upstate Medical University, Syracuse, New York, USA duttad@upstate.edu gargri@upstate.edu.<br /><searchLink fieldCode="AU" term="%22Black+J%22">Black J</searchLink>; Center of Development, Behavior, and Genetics, SUNY Upstate Medical University, Syracuse, New York, USA.<br /><searchLink fieldCode="AU" term="%22Montoya+EA%22">Montoya EA</searchLink>; Department of Pediatrics, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.<br /><searchLink fieldCode="AU" term="%22Burrow+TA%22">Burrow TA</searchLink>; Department of Pediatrics, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.<br /><searchLink fieldCode="AU" term="%22Shieh+J%22">Shieh J</searchLink>; Division of Medical Genetics, Department of Pediatrics, University of California San Francisco, San Francisco, California, USA.<br /><searchLink fieldCode="AU" term="%22McGivern+B%22">McGivern B</searchLink>; GeneDx, Gaithersburg, Maryland, USA.<br /><searchLink fieldCode="AU" term="%22Raymond+M%22">Raymond M</searchLink>; GeneDx, Gaithersburg, Maryland, USA.<br /><searchLink fieldCode="AU" term="%22Sheedy+CB%22">Sheedy CB</searchLink>; GeneDx, Gaithersburg, Maryland, USA.<br /><searchLink fieldCode="AU" term="%22Smith+SC%22">Smith SC</searchLink>; Department of Pathology, SUNY Upstate Medical University, Syracuse, New York, USA.<br /><searchLink fieldCode="AU" term="%22Garg+R%22">Garg R</searchLink>; Center of Development, Behavior, and Genetics, SUNY Upstate Medical University, Syracuse, New York, USA duttad@upstate.edu gargri@upstate.edu. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%222985087R%22">Journal of medical genetics</searchLink> [J Med Genet] 2025 Mar 20; Vol. 62 (4), pp. 268-275. <i>Date of Electronic Publication: </i>2025 Mar 20. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22British+Medical+Association%22">British Medical Association </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>2985087R <i>Publication Model: </i>Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1468-6244 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2200222593%22">00222593 </searchLink><i>NLM ISO Abbreviation: </i>J Med Genet <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=39904608 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1136/jmg-2024-110367 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 268 Titles: – TitleFull: Neurodevelopmental delay, musculoskeletal disorders and dysmorphia associated with a novel pathogenic interstitial deletion of chromosome 10q21.1q21.3. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Dutta D – PersonEntity: Name: NameFull: Black J – PersonEntity: Name: NameFull: Montoya EA – PersonEntity: Name: NameFull: Burrow TA – PersonEntity: Name: NameFull: Shieh J – PersonEntity: Name: NameFull: McGivern B – PersonEntity: Name: NameFull: Raymond M – PersonEntity: Name: NameFull: Sheedy CB – PersonEntity: Name: NameFull: Smith SC – PersonEntity: Name: NameFull: Garg R IsPartOfRelationships: – BibEntity: Dates: – D: 20 M: 03 Text: 2025 Mar 20 Type: published Y: 2025 Identifiers: – Type: issn-electronic Value: 1468-6244 Numbering: – Type: volume Value: 62 – Type: issue Value: 4 Titles: – TitleFull: Journal of medical genetics Type: main |
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