Works matching IS 03406717 AND DT 2021 AND VI 140 AND IP 1
Results: 13
Editorial for the special issue on the molecular genetics of male infertility.
- Published in:
- 2021
- By:
- Publication type:
- Editorial
Correction to: Disruption of human meiotic telomere complex genes TERB1, TERB2 and MAJIN in men with non-obstructive azoospermia.
- Published in:
- 2021
- By:
- Publication type:
- Correction Notice
Disruption of human meiotic telomere complex genes TERB1, TERB2 and MAJIN in men with non-obstructive azoospermia.
- Published in:
- Human Genetics, 2021, v. 140, n. 1, p. 217, doi. 10.1007/s00439-020-02236-1
- By:
- Publication type:
- Article
Genetic analyses of a large cohort of infertile patients with globozoospermia, DPY19L2 still the main actor, GGN confirmed as a guest player.
- Published in:
- Human Genetics, 2021, v. 140, n. 1, p. 43, doi. 10.1007/s00439-020-02229-0
- By:
- Publication type:
- Article
Disease gene discovery in male infertility: past, present and future.
- Published in:
- Human Genetics, 2021, v. 140, n. 1, p. 7, doi. 10.1007/s00439-020-02202-x
- By:
- Publication type:
- Article
A framework for high-resolution phenotyping of candidate male infertility mutants: from human to mouse.
- Published in:
- Human Genetics, 2021, v. 140, n. 1, p. 155, doi. 10.1007/s00439-020-02159-x
- By:
- Publication type:
- Article
Molecular genetic diagnostics of hypogonadotropic hypogonadism: from panel design towards result interpretation in clinical practice.
- Published in:
- Human Genetics, 2021, v. 140, n. 1, p. 113, doi. 10.1007/s00439-020-02148-0
- By:
- Publication type:
- Article
Genetics of congenital hypogonadotropic hypogonadism: peculiarities and phenotype of an oligogenic disease.
- Published in:
- Human Genetics, 2021, v. 140, n. 1, p. 77, doi. 10.1007/s00439-020-02147-1
- By:
- Publication type:
- Article
Genetics of the congenital absence of the vas deferens.
- Published in:
- Human Genetics, 2021, v. 140, n. 1, p. 59, doi. 10.1007/s00439-020-02122-w
- By:
- Publication type:
- Article
Evaluating genetic causes of azoospermia: What can we learn from a complex cellular structure and single-cell transcriptomics of the human testis?
- Published in:
- Human Genetics, 2021, v. 140, n. 1, p. 183, doi. 10.1007/s00439-020-02116-8
- By:
- Publication type:
- Article
The genetic architecture of morphological abnormalities of the sperm tail.
- Published in:
- Human Genetics, 2021, v. 140, n. 1, p. 21, doi. 10.1007/s00439-020-02113-x
- By:
- Publication type:
- Article
Monogenic causes of non-obstructive azoospermia: challenges, established knowledge, limitations and perspectives.
- Published in:
- Human Genetics, 2021, v. 140, n. 1, p. 135, doi. 10.1007/s00439-020-02112-y
- By:
- Publication type:
- Article
The X chromosome and male infertility.
- Published in:
- Human Genetics, 2021, v. 140, n. 1, p. 203, doi. 10.1007/s00439-019-02101-w
- By:
- Publication type:
- Article