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Variants in genes related to development of the urinary system are associated with Mayer–Rokitansky–Küster–Hauser syndrome.
- Published in:
- Human Genomics, 2022, v. 16, n. 1, p. 1, doi. 10.1186/s40246-022-00385-0
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- Article
A novel EIF4ENIF1 mutation associated with a diminished ovarian reserve and premature ovarian insufficiency identified by whole-exome sequencing.
- Published in:
- Journal of Ovarian Research, 2019, v. 12, n. 1, p. N.PAG, doi. 10.1186/s13048-019-0595-0
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- Article
Correction: TP63 truncating mutation causes increased cell apoptosis and premature ovarian insufficiency by enhanced transcriptional activation of CLCA2.
- Published in:
- 2024
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- Correction Notice
TP63 truncating mutation causes increased cell apoptosis and premature ovarian insufficiency by enhanced transcriptional activation of CLCA2.
- Published in:
- Journal of Ovarian Research, 2024, v. 17, n. 1, p. 1, doi. 10.1186/s13048-024-01396-2
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- Article