18 results on '"Shao, Zhongmei"'
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2. Association of FOXL2 and ERCC6 variants with premature ovarian insufficiency and their potential use in clinical IVF guidance
3. Correction to: Homozygous SPAG6 variants can induce nonsyndromic asthenoteratozoospermia with severe MMAF
4. Homozygous SPAG6 variants can induce nonsyndromic asthenoteratozoospermia with severe MMAF
5. Correction: Identification of deleterious variants in patients with male infertility due to idiopathic non-obstructive azoospermia
6. Identification of deleterious variants in patients with male infertility due to idiopathic non-obstructive azoospermia
7. Homozygous mutation in SLO3 leads to severe asthenoteratozoospermia due to acrosome hypoplasia and mitochondrial sheath malformations
8. Bi-allelic variants in DNAH10 cause asthenoteratozoospermia and male infertility
9. Identification of deleterious variants in nine polycystic kidney disease affected families
10. Novel HYDIN variants associated with male infertility in two Chinese families
11. Novel FSIP2 Variants Induce Super-Length Mitochondrial Sheath and Asthenoteratozoospermia in Humans
12. Additional file 2 of Homozygous SPAG6 variants can induce nonsyndromic asthenoteratozoospermia with severe MMAF
13. Additional file 1 of Homozygous SPAG6 variants can induce nonsyndromic asthenoteratozoospermia with severe MMAF
14. Additional file 1 of Homozygous mutation in SLO3 leads to severe asthenoteratozoospermia due to acrosome hypoplasia and mitochondrial sheath malformations
15. Additional file 4 of Homozygous SPAG6 variants can induce nonsyndromic asthenoteratozoospermia with severe MMAF
16. Additional file 5 of Homozygous SPAG6 variants can induce nonsyndromic asthenoteratozoospermia with severe MMAF
17. Homozygous SPAG6 Variants Can Induce Nonsyndromic Asthenoteratozoospermia With Severe MMAF
18. Bi-allelic variants in DNAH10 cause asthenoteratozoospermia and male infertility
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