GREB1L as a candidate gene of Mayer–Rokitansky–Küster–Hauser Syndrome
Author:
Publisher
Elsevier BV
Subject
Genetics(clinical),Genetics,General Medicine
Reference67 articles.
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1. Research on the shared function of central neurons and breast cancer based on gene expression profile data mining: The role of EMID1 protein antibody expression;International Journal of Biological Macromolecules;2024-10
2. A novel de novo synonymous variant in GREB1L impacts the mRNA splicing associated with aplasia of the urogenital system;American Journal of Medical Genetics Part A;2024-08-02
3. Murcs Association: A most severe form of Mayer-Rokitansky-Küster-Hauser Syndrome, case report and literature review;Journal of IVF-Worldwide;2024-07-30
4. Molecular Basis of Müllerian Agenesis Causing Congenital Uterine Factor Infertility—A Systematic Review;International Journal of Molecular Sciences;2023-12-21
5. Rare variant enrichment analysis supports GREB1L as a contributory driver gene in the etiology of Mayer-Rokitansky-Küster-Hauser syndrome;Human Genetics and Genomics Advances;2023-07
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