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(1994) Highly homologous loci on the X and Y chromosomes are hot-spots for ectopic recombinations leading to XX maleness. Nat Genet<\/i> 7: 414-419.","DOI":"10.1038\/ng0794-414"},{"key":"5","doi-asserted-by":"crossref","unstructured":"5. Wang I, Weil D, Levilliers J, Affara NA, de la Chapelle A, et al. (1995) Prevalence and molecular analysis of two hot spots for ectopic recombination leading to XX maleness. Genomics<\/i>28: 52-58.","DOI":"10.1006\/geno.1995.1105"},{"key":"6","doi-asserted-by":"crossref","unstructured":"6. Schiebel K, Winkelmann M, Mertz A, Xu X, Page DC, et al. (1997) Abnormal XY interchange between a novel isolated protein kinase gene, PRKY, and its homologue, PRKX, accounts for one third of all (Y+)XX males and (Y-)XY females. Hum Mol Genet<\/i> 6: 1985-1989.","DOI":"10.1093\/hmg\/6.11.1985"},{"key":"7","doi-asserted-by":"crossref","unstructured":"7. Jobling MA, Williams GA, Schiebel GA Pandya GA, McElreavey GA, et al. (1998) A selective difference between human Y-chromosomal DNA haplotypes. Curr Biol<\/i> 8: 1391-1394.","DOI":"10.1016\/S0960-9822(98)00020-7"},{"key":"8","doi-asserted-by":"crossref","unstructured":"8. Tilford CA, Kuroda-Kawaguchi T, Skaletsky H, Rozen S, Brown LG, et al. (2001) A physical map of the human Y chromosome. Nature<\/i> 409: 943-945.","DOI":"10.1038\/35057170"},{"key":"9","doi-asserted-by":"crossref","unstructured":"9. Sharp A, Kusz K, Jaruzelska J, Tapper W, Szarras-Czapnik M, et al. (2005) Variability of sexual phenotype in 46,XX(SRY+) patients: the influence of spreading X inactivation versus position effects. J Med Genet<\/i> 42: 420-427.","DOI":"10.1136\/jmg.2004.022053"},{"key":"10","doi-asserted-by":"crossref","unstructured":"10. McElreavey K, Cortes LS (2001) X-Y translocations and sex differentiation. Semin Reprod Med<\/i> 19: 133-139.","DOI":"10.1055\/s-2001-15393"},{"key":"11","doi-asserted-by":"crossref","unstructured":"11. Sinclair AH, Berta P, Palmer MS, Hawkins JR, Griffiths BL, et al. (1990) A gene from the human sex-determining region encodes a protein with homology to a conserved DNA-binding motif. Nature<\/i> 346: 240-244.","DOI":"10.1038\/346240a0"},{"key":"12","doi-asserted-by":"crossref","unstructured":"12. Franco B, Meroni G, Parenti G, Levilliers J, Bernard L, et al. (1995) A cluster of sulfatase genes on Xp22.3: mutations in chondrodysplasia punctata (CDPX) and implications for warfarin embryopathy. Cell<\/i> 81: 15-25.","DOI":"10.1016\/0092-8674(95)90367-4"},{"key":"13","doi-asserted-by":"crossref","unstructured":"13. Ogata T, Matsuo N (1993) Sex chromosome aberrations and stature: deduction of the principal factors involved in the determination of adult height. Hum Genet<\/i> 91: 551-562.","DOI":"10.1007\/BF00205079"},{"key":"14","doi-asserted-by":"crossref","unstructured":"14. Rao E, Weiss B, Fukami M, Rump A, Niesler B, et al. (1997) Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome. Nat Genet<\/i> 16: 54-63.","DOI":"10.1038\/ng0597-54"},{"key":"15","doi-asserted-by":"crossref","unstructured":"15. Ogata T, Matsuo N (1995) Turner syndrome and female sex chromosome aberrations: deduction of the principal factors involved in the development of clinical features. Hum Genet<\/i> 95: 607-629.","DOI":"10.1007\/BF00209476"},{"key":"16","doi-asserted-by":"crossref","unstructured":"16. Ogata T, Muroya K, Matsuo N, Shinohara O, Yorifuji T, et al. (2001) Turner syndrome and Xp deletions: clinical and molecular studies in 47 patients. J Clin Endocrinol Metab<\/i> 86: 5498-5508.","DOI":"10.1210\/jcem.86.11.8058"},{"key":"17","doi-asserted-by":"crossref","unstructured":"17. Ogata T, Tyler-Smith C, Purvis-Smith S, Turner G (1993) Chromosomal localisation of a gene(s) for Turner stigmata on Yp. 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