Identification of rare genetic variants in the PCDH genetic family in a cohort of transgender women.
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| Title: | Identification of rare genetic variants in the PCDH genetic family in a cohort of transgender women. |
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| Authors: | Theisen JG; Section of Reproductive Endocrinology, Infertility, and Genetics, Department of Obstetrics and Gynecology, Medical College of Georgia, Augusta University, Augusta, Georgia. Electronic address: jtheisen@augusta.edu., Chorich LP; Section of Reproductive Endocrinology, Infertility, and Genetics, Department of Obstetrics and Gynecology, Medical College of Georgia, Augusta University, Augusta, Georgia., Xu H; Section of Reproductive Endocrinology, Infertility, and Genetics, Department of Obstetrics and Gynecology, Medical College of Georgia, Augusta University, Augusta, Georgia., Knight J; Department of Genetics, Yale University School of Medicine, New Haven, Connecticut; Yale Center for Genome Analysis, Yale University, New Haven, Connecticut., Kim HG; Department of Neurosurgery, Robert Wood Johnson Medical School, Rutgers University, New Jersey, New Jersey., Layman LC; Section of Reproductive Endocrinology, Infertility, and Genetics, Department of Obstetrics and Gynecology, Medical College of Georgia, Augusta University, Augusta, Georgia; Department of Neuroscience and Regenerative Medicine, Medical College of Georgia, Augusta University, Augusta, Georgia; Department of Physiology, Medical College of Georgia, Augusta University, Augusta, Georgia. |
| Source: | F&S science [F S Sci] 2024 Aug; Vol. 5 (3), pp. 283-292. Date of Electronic Publication: 2024 Jun 26. |
| Publication Type: | Journal Article; Research Support, N.I.H., Extramural |
| Journal Info: | Publisher: Elsevier Inc Country of Publication: United States NLM ID: 101765857 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2666-335X (Electronic) Linking ISSN: 2666335X NLM ISO Abbreviation: F S Sci Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 38942387 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Identification of rare genetic variants in the PCDH genetic family in a cohort of transgender women. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Theisen+JG%22">Theisen JG</searchLink>; Section of Reproductive Endocrinology, Infertility, and Genetics, Department of Obstetrics and Gynecology, Medical College of Georgia, Augusta University, Augusta, Georgia. Electronic address: jtheisen@augusta.edu.<br /><searchLink fieldCode="AU" term="%22Chorich+LP%22">Chorich LP</searchLink>; Section of Reproductive Endocrinology, Infertility, and Genetics, Department of Obstetrics and Gynecology, Medical College of Georgia, Augusta University, Augusta, Georgia.<br /><searchLink fieldCode="AU" term="%22Xu+H%22">Xu H</searchLink>; Section of Reproductive Endocrinology, Infertility, and Genetics, Department of Obstetrics and Gynecology, Medical College of Georgia, Augusta University, Augusta, Georgia.<br /><searchLink fieldCode="AU" term="%22Knight+J%22">Knight J</searchLink>; Department of Genetics, Yale University School of Medicine, New Haven, Connecticut; Yale Center for Genome Analysis, Yale University, New Haven, Connecticut.<br /><searchLink fieldCode="AU" term="%22Kim+HG%22">Kim HG</searchLink>; Department of Neurosurgery, Robert Wood Johnson Medical School, Rutgers University, New Jersey, New Jersey.<br /><searchLink fieldCode="AU" term="%22Layman+LC%22">Layman LC</searchLink>; Section of Reproductive Endocrinology, Infertility, and Genetics, Department of Obstetrics and Gynecology, Medical College of Georgia, Augusta University, Augusta, Georgia; Department of Neuroscience and Regenerative Medicine, Medical College of Georgia, Augusta University, Augusta, Georgia; Department of Physiology, Medical College of Georgia, Augusta University, Augusta, Georgia. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22101765857%22">F&S science</searchLink> [F S Sci] 2024 Aug; Vol. 5 (3), pp. 283-292. <i>Date of Electronic Publication: </i>2024 Jun 26. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article; Research Support, N.I.H., Extramural – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Elsevier+Inc%22">Elsevier Inc </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>101765857 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>2666-335X (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%222666335X%22">2666335X </searchLink><i>NLM ISO Abbreviation: </i>F S Sci <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=38942387 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1016/j.xfss.2024.06.005 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 283 Titles: – TitleFull: Identification of rare genetic variants in the PCDH genetic family in a cohort of transgender women. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Theisen JG – PersonEntity: Name: NameFull: Chorich LP – PersonEntity: Name: NameFull: Xu H – PersonEntity: Name: NameFull: Knight J – PersonEntity: Name: NameFull: Kim HG – PersonEntity: Name: NameFull: Layman LC IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 08 Text: 2024 Aug Type: published Y: 2024 Identifiers: – Type: issn-electronic Value: 2666-335X Numbering: – Type: volume Value: 5 – Type: issue Value: 3 Titles: – TitleFull: F&S science Type: main |
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