Identification of rare genetic variants in the PCDH genetic family in a cohort of transgender women.

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Bibliographic Details
Title: Identification of rare genetic variants in the PCDH genetic family in a cohort of transgender women.
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
Description
ISSN:2666-335X
DOI:10.1016/j.xfss.2024.06.005