Partial deletion of DMRT1 causes 46,XY ovotesticular disorder of sexual development
Author:
Publisher
Bioscientifica
Subject
Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism
Reference35 articles.
1. True hermaphroditism: Geographical distribution, clinical findings, chromosomes and gonadal histology
2. AN XX/XY HUMAN HERMAPHRODITE RESULTING FROM DOUBLE FERTILIZATION
3. Chimera and other fertilization errors
4. The role of the sex-determining region of the Y chromosome (SRY) in the etiology of 46,XX true hermaphroditism
5. Partially deleted SRY gene confined to testicular tissue in a 46,XX true hermaphrodite without SRY in leukocytic DNA
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1. DMRT1 is a testis-determining gene in rabbits and is also essential for female fertility;eLife;2023-10-17
2. DMRT1 is a testis-determining gene in rabbits and is also essential for female fertility;eLife;2023-10-17
3. Nuclear Receptor Gene Variants Underlying Disorders/Differences of Sex Development through Abnormal Testicular Development;Biomolecules;2023-04-19
4. Functional assessment of DMRT1 variants and their pathogenicity for isolated male infertility;Fertility and Sterility;2023-02
5. Inherited deletion of 9p22.3‐p24.3 and duplication of 18p11.31‐p11.32 associated with neurodevelopmental delay: Phenotypic matching of involved genes;Journal of Cellular and Molecular Medicine;2023-01-24
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