Found: 7
Select item for more details and to access through your institution.
A homozygous missense variant in YTHDC2 induces azoospermia in two siblings.
- Published in:
- Molecular Genetics & Genomics, 2024, v. 299, n. 1, p. 1, doi. 10.1007/s00438-024-02168-9
- By:
- Publication type:
- Article
Novel Mutations in X-Linked, USP26 -Induced Asthenoteratozoospermia and Male Infertility.
- Published in:
- Cells (2073-4409), 2021, v. 10, n. 7, p. 1594, doi. 10.3390/cells10071594
- By:
- Publication type:
- Article
A novel hemizygous loss-of-function mutation in ADGRG2 causes male infertility with congenital bilateral absence of the vas deferens.
- Published in:
- Journal of Assisted Reproduction & Genetics, 2020, v. 37, n. 6, p. 1421, doi. 10.1007/s10815-020-01779-6
- By:
- Publication type:
- Article
A novel homozygous mutation in WDR19 induces disorganization of microtubules in sperm flagella and nonsyndromic asthenoteratospermia.
- Published in:
- Journal of Assisted Reproduction & Genetics, 2020, v. 37, n. 6, p. 1431, doi. 10.1007/s10815-020-01770-1
- By:
- Publication type:
- Article
Deficiency of X-linked TENT5D causes male infertility by disrupting the mRNA stability during spermatogenesis.
- Published in:
- 2022
- By:
- Publication type:
- Letter
Deleterious variant in FAM71D cause male infertility with asthenoteratospermia.
- Published in:
- Molecular Genetics & Genomics, 2024, v. 299, n. 1, p. 1, doi. 10.1007/s00438-024-02117-6
- By:
- Publication type:
- Article
NGS-driven molecular diagnosis of heterogeneous hereditary neurological disorders reveals novel and known variants in disease-causing genes.
- Published in:
- Molecular Genetics & Genomics, 2022, v. 297, n. 6, p. 1601, doi. 10.1007/s00438-022-01945-8
- By:
- Publication type:
- Article