On the origins and fate of chromosomal abnormalities in human preimplantation embryos: an unsolved riddle.
- Published in:
- Molecular Human Reproduction, 2022, v. 28, n. 4, p. 1, doi. 10.1093/molehr/gaac011
- By:
- Publication type:
- Article
Works matching IS 13609947 AND DT 2022 AND VI 28 AND IP 4
Results: 4
1
2
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
- By:
- Publication type:
- Article
3
reproductive science perspective: deliberations on the stem cell guidelines update.
- Published in:
- Molecular Human Reproduction, 2022, v. 28, n. 4, p. 1, doi. 10.1093/molehr/gaac008
- By:
- Publication type:
- Article
4
Inhibition of the NLRP3 inflammasome by progesterone is attenuated by abnormal autophagy induction in endometriotic cyst stromal cells: implications for endometriosis.
- Published in:
- Molecular Human Reproduction, 2022, v. 28, n. 4, p. 1, doi. 10.1093/molehr/gaac007
- By:
- Publication type:
- Article