Found: 8
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rare frameshift mutation in SYCP1 is associated with human male infertility.
- Published in:
- Molecular Human Reproduction, 2022, v. 28, n. 4, p. 1, doi. 10.1093/molehr/gaac009
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- Publication type:
- Article
Strategies for whole-exome sequencing analysis in a case series study of familial male infertility.
- Published in:
- International Journal of Reproductive Biomedicine, 2020, v. 18, n. 5, p. 375, doi. 10.18502/ijrm.v13i5.7158
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- Publication type:
- Article
Expanding DSD Phenotypes Associated with Variants in the DEAH-Box RNA Helicase DHX37.
- Published in:
- Sexual Development, 2021, v. 15, n. 4, p. 244, doi. 10.1159/000515924
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- Publication type:
- Article
Novel MYO15A variants are associated with hearing loss in the two Iranian pedigrees.
- Published in:
- BMC Medical Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s12881-020-01168-x
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- Publication type:
- Article
A systematic review and meta-analysis for the association of the insulin-like growth factor1 pathway genetic polymorphisms with colorectal cancer susceptibility.
- Published in:
- Frontiers in Oncology, 2023, p. 1, doi. 10.3389/fonc.2023.1168942
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- Publication type:
- Article
Claudin-2 deficiency associates with hypercalciuria in mice and human kidney stone disease.
- Published in:
- 2020
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- Publication type:
- journal article
A missense mutation in NR5A1 causing female to male sex reversal: A case report.
- Published in:
- Andrologia, 2020, v. 52, n. 6, p. 1, doi. 10.1111/and.13585
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- Publication type:
- Article
Rare case of an oligospermic male with 46,XX/46,XY tetragametic chimerism.
- Published in:
- Andrologia, 2019, v. 51, n. 7, p. N.PAG, doi. 10.1111/and.13290
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- Publication type:
- Article