Page 246 - Remedial Andrology

1551. Zhang, F., et al. Partial deletions are associated with an increased risk of complete deletion in AZFc:
a new insight into the role of partial AZFc deletions in male infertility. J Med Genet, 2007. 44: 437.
https://pubmed.ncbi.nlm.nih.gov/17412880
1552. Haltrich, I. Chromosomal Aberrations with Endocrine Relevance (Turner Syndrome, Klinefelter
Syndrome, Prader-Willi Syndrome). Exp Suppl, 2019. 111: 443.
https://pubmed.ncbi.nlm.nih.gov/31588543
1553. Tsang, S.H., et al. Ciliopathy: Bardet-Biedl Syndrome. Adv Exp Med Biol, 2018. 1085: 171.
https://pubmed.ncbi.nlm.nih.gov/30578506
1554. Mieusset, R., et al. The spectrum of renal involvement in male patients with infertility related to
excretory-system abnormalities: phenotypes, genotypes, and genetic counseling. J Nephrol, 2017.
30: 211.
https://pubmed.ncbi.nlm.nih.gov/26946416
1555. Luciano, R.L., et al. Extra-renal manifestations of autosomal dominant polycystic kidney disease
(ADPKD): considerations for routine screening and management. Nephrol Dial Transplant, 2014.
29: 247.
https://pubmed.ncbi.nlm.nih.gov/24215018
1556. Van Batavia, J.P., et al. Fertility in disorders of sex development: A review. J Pediatr Urol, 2016.
12: 418.
https://pubmed.ncbi.nlm.nih.gov/27856173
1557. Kosti, K., et al. Long-term consequences of androgen insensitivity syndrome. Maturitas, 2019. 127:
51.
https://pubmed.ncbi.nlm.nih.gov/31351520
1558. Hsieh, M.H., et al. The genetic and phenotypic basis of infertility in men with pediatric urologic
disorders. Urology, 2010. 76: 25.
https://pubmed.ncbi.nlm.nih.gov/20451977
1559. Okutman, O., et al. Genetic evaluation of patients with non-syndromic male infertility. J Assist
Reprod Genet, 2018. 35: 1939.
https://pubmed.ncbi.nlm.nih.gov/30259277
1560. Luo, K., et al. Next-generation sequencing analysis of embryos from mosaic patients undergoing in
vitro fertilization and preimplantation genetic testing. Fertil Steril, 2019. 112: 291.
https://pubmed.ncbi.nlm.nih.gov/31133385
1561. Kohn, T.P., et al. Reproductive outcomes in men with karyotype abnormalities: Case report and
review of the literature. Can Urol Ass J, 2015. 9: E667.
https://pubmed.ncbi.nlm.nih.gov/26425238
1562. Gianaroli, L., et al. Frequency of aneuploidy in sperm from patients with extremely severe male
factor infertility. Hum Reprod, 2005. 20: 2140.
https://pubmed.ncbi.nlm.nih.gov/15845594
1563. Pang, M.G., et al. The high incidence of meiotic errors increases with decreased sperm count in
severe male factor infertilities. Hum Reprod, 2005. 20: 1688.
https://pubmed.ncbi.nlm.nih.gov/15734753
1564. Tempest, H.G., et al. Cytogenetic risks in chromosomally normal infertile men. Curr Opin Obstet
Gynecol, 2009. 21: 223.
https://pubmed.ncbi.nlm.nih.gov/19424064
1565. Baccetti, B., et al. Ultrastructural studies of spermatozoa from infertile males with Robertsonian
translocations and 18, X, Y aneuploidies. Hum Reprod, 2005. 20: 2295.
https://pubmed.ncbi.nlm.nih.gov/15878922
1566. Rodrigo, L., et al. Sperm chromosomal abnormalities and their contribution to human embryo
aneuploidy. Biol Reprod, 2019. 101: 1091.
https://pubmed.ncbi.nlm.nih.gov/31318411
1567. Agarwal, A., et al. Sperm DNA damage assessment: a test whose time has come. Fertil Steril, 2005.
84: 850.
https://pubmed.ncbi.nlm.nih.gov/16213833
1568. Zini, A., et al. Correlations between two markers of sperm DNA integrity, DNA denaturation and DNA
fragmentation, in fertile and infertile men. Fertil Steril, 2001. 75: 674.
https://pubmed.ncbi.nlm.nih.gov/11287017
1569. Iommiello, V.M., et al. Ejaculate oxidative stress is related with sperm DNA fragmentation and round
cells. Int J Endocrinol, 2015. 2015: 321901.
https://pubmed.ncbi.nlm.nih.gov/25802519
1570. Bisht, S., et al. Oxidative stress and male infertility. Nat Rev Urol, 2017. 14: 470.
https://pubmed.ncbi.nlm.nih.gov/28508879

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