Page 244 - Remedial Andrology
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1510.   Ferlin, A., et al. Contemporary genetics-based diagnostics of male infertility. Expert Rev Mol Diagn,
                                2019. 19: 623.
                                https://pubmed.ncbi.nlm.nih.gov/31215260
                        1511.   Nguyen, M.H., et al. Balanced complex chromosome rearrangement in male infertility: case report
                                and literature review. Andrologia, 2015. 47: 178.
                                https://onlinelibrary.wiley.com/doi/abs/10.1111/and.12245
                        1512.   Siffroi, J.P., et al. Assisted reproductive technology and complex chromosomal rearrangements: the
                                limits of ICSI. Mol Hum Reprod, 1997. 3: 847.
                                https://pubmed.ncbi.nlm.nih.gov/9395262
                        1513.   De Boeck, K. Cystic fibrosis in the year 2020: a disease with a new face. Acta Paediatr, 2020.
                                https://pubmed.ncbi.nlm.nih.gov/31899933
                        1514.   McBride, J.A.,  et al. Sperm retrieval and intracytoplasmic sperm injection outcomes in men with
                                cystic fibrosis disease versus congenital bilateral absence of the vas deferens. Asian J Androl, 2020.
                                https://pubmed.ncbi.nlm.nih.gov/32930103
                        1515.   Donat, R., et al. The incidence of cystic fibrosis gene mutations in patients with congenital bilateral
                                absence of the vas deferens in Scotland. Br J Urol, 1997. 79: 74.
                                https://pubmed.ncbi.nlm.nih.gov/9043501
                        1516.   Practice Committee of the American Society for Reproductive, M. Diagnostic evaluation of the
                                infertile male: a committee opinion. Fertil Steril, 2015. 103: e18.
                                https://pubmed.ncbi.nlm.nih.gov/25597249
                        1517.   Oates, R. Evaluation of the azoospermic male. Asian J Androl, 2012. 14: 82.
                                https://pubmed.ncbi.nlm.nih.gov/22179510
                        1518.   Daudin, M., et al. Congenital bilateral absence of the vas deferens: clinical characteristics, biological
                                parameters, cystic fibrosis transmembrane conductance regulator gene mutations, and implications
                                for genetic counseling. Fertil Steril, 2000. 74: 1164.
                                https://pubmed.ncbi.nlm.nih.gov/11119745
                        1519.   Chillon, M., et al. Mutations in the cystic fibrosis gene in patients with congenital absence of the vas
                                deferens. N Engl J Med, 1995. 332: 1475.
                                https://pubmed.ncbi.nlm.nih.gov/7739684
                        1520.   De Braekeleer, M.,  et al. Mutations in the cystic fibrosis gene in men with congenital bilateral
                                absence of the vas deferens. Mol Hum Reprod, 1996. 2: 669.
                                https://pubmed.ncbi.nlm.nih.gov/9239681
                        1521.   Nathanson, K.L.,  et al. The Y deletion gr/gr and susceptibility to testicular germ cell tumor. Am
                                 J Hum Genet, 2005. 77: 1034.
                                https://pubmed.ncbi.nlm.nih.gov/16380914
                        1522.   Krausz, C., et al. Genetic risk factors in male infertility. Arch Androl, 2007. 53: 125.
                                https://pubmed.ncbi.nlm.nih.gov/17612870
                        1523.   Augarten, A., et al. Congenital bilateral absence of vas deferens in the absence of cystic fibrosis.
                                Lancet, 1994. 344: 1473.
                                https://pubmed.ncbi.nlm.nih.gov/7968122
                        1524.   Schlegel, P.N.,  et al. Urogenital anomalies in men with congenital absence of the vas deferens.
                                J Urol, 1996. 155: 1644.
                                https://pubmed.ncbi.nlm.nih.gov/8627844
                        1525.   Drake, M.J., et al. Absent vas deferens and ipsilateral multicystic dysplastic kidney in a child. Br
                                J Urol, 1996. 77: 756.
                                https://pubmed.ncbi.nlm.nih.gov/8689131
                        1526.   Vogt, P.H., et al. Human Y chromosome azoospermia factors (AZF) mapped to different subregions
                                in Yq11. Hum Mol Genet, 1996. 5: 933.
                                https://pubmed.ncbi.nlm.nih.gov/8817327
                        1527.   Krausz, C., et al. Spermatogenic failure and the Y chromosome. Hum Genet, 2017. 136: 637.
                                https://pubmed.ncbi.nlm.nih.gov/28456834
                        1528.   Skaletsky, H., et al. The male-specific region of the human Y chromosome is a mosaic of discrete
                                sequence classes. Nature, 2003. 423: 825.
                                https://pubmed.ncbi.nlm.nih.gov/12815422
                        1529.   Tyler-Smith, C.,  et al. The will-o’-the-wisp of genetics--hunting for the azoospermia factor gene.
                                N Engl J Med, 2009. 360: 925.
                                https://pubmed.ncbi.nlm.nih.gov/19246366
                        1530.   Stouffs, K., et al. Are AZFb deletions always incompatible with sperm production? Andrology, 2017.
                                5: 691.
                                https://pubmed.ncbi.nlm.nih.gov/28395120




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