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Lange,              J, Skaletsky,                H, van                Daalen, SK,                Embry, SL,                Korver, CM,                Brown, LG,              et al. Isodicentric Y chromosomes and sex            disorders as byproducts of homologous recombination that maintains            palindromes. Cell          2009;138: 855\u201369.","DOI":"10.1016\/j.cell.2009.07.042"},{"key":"2","doi-asserted-by":"crossref","unstructured":"2. Quilter,                CR,                Nathwani,            N, Conway,                GS,                Stanhope,            R, Ralph,                D, Bahadur,                G, et al.            A comparative study between infertile males and patients with Turner            syndrome to determine the influence of sex chromosome mosaicism and the breakpoints of            structurally abnormal Y chromosomes on phenotypic sex. J Med            Genet          2002;39: e80.","DOI":"10.1136\/jmg.39.12.e80"},{"key":"3","unstructured":"3. Gole,              LA, Lim,                J, Crolla,                JA, Loke,                KY. Gonadal            mosaicism 45,X\/46,X,psu dic(Y)(q11.2) resulting in a Turner phenotype with mixed gonadal            dysgenesis. Singapore Med J          2008;49: 349\u201351."},{"key":"4","doi-asserted-by":"crossref","unstructured":"4. Jobling,                MA,                Tyler-Smith,              C. Human            Y-chromosome variation in the genome-sequencing era. Nat Rev            Genet          2017;18: 485\u201397.","DOI":"10.1038\/nrg.2017.36"},{"key":"5","doi-asserted-by":"crossref","unstructured":"5. Reshmi,              SC, Miller,                JL,                Deplewski,              D, Close,                C,                Henderson,              LJ,                Littlejohn,              E, et al.            Evidence of a mechanism for isodicentric chromosome Y formation in a            45,X\/46,X,idic(Y)(p11.31)\/46,X,del(Y)(p11.31) mosaic karyotype.            Eur J Med Genet          2011;54: 161\u20134.","DOI":"10.1016\/j.ejmg.2010.11.002"},{"key":"6","doi-asserted-by":"publisher","unstructured":"6. Skaletsky,                H,                Kuroda-Kawaguchi,              T, Minx,                PJ, Cordum,                HS,              Hillier, L,                Brown, LG,              et al. The male-specific region of the            human Y chromosome is a mosaic of discrete sequence classes.            Nature          2003;423: 825\u201337.","DOI":"10.1038\/nature01722"},{"key":"7","doi-asserted-by":"crossref","unstructured":"7. Miyado,              M, Muroya,                K, Katsumi,                M, Saito,                K, Kon,                M, Fukami,                M.            Somatically acquired isodicentric Y and mosaic loss of chromosome Y in a            boy with hypospadias. Cytogenet Genome Res          2018;154: 122\u20135.","DOI":"10.1159\/000488162"},{"key":"8","doi-asserted-by":"crossref","unstructured":"8. Kosho,              T, Muroya,                K, Nagai,                T,              Fujimoto, M,                Yokoya, S,                Sakamoto,            H, et al.            Skeletal features and growth patterns in 14 patients with            haploinsufficiency of SHOX: implications for the development of Turner            syndrome. J Clin Endocrinol Metab          1999;84: 4613\u201321.","DOI":"10.1210\/jcem.84.12.6289"},{"key":"9","doi-asserted-by":"crossref","unstructured":"9. Rao,              E, Weiss,                B, Fukami,                M, Rump,                A, Niesler,                B, Mertz,                A, et al.            Pseudoautosomal deletions encompassing a novel homeobox gene cause growth            failure in idiopathic short stature and Turner syndrome. Nat            Genet          1997;16: 54\u201363.","DOI":"10.1038\/ng0597-54"},{"key":"10","unstructured":"10. Ogata,              T, Matsuo,                N. The Y            specific growth gene(s): how does it promote stature? J Med            Genet          1997;34: 323\u20135."},{"key":"11","doi-asserted-by":"crossref","unstructured":"11. Kirsch,              S, Weiss,                B, De Rosa,                M, Ogata,                T,              Lombardi, G,                Rappold,            GA. FISH deletion            mapping defines a single location for the Y chromosome stature gene,          GCY. J Med Genet          2000;37: 593\u20139.","DOI":"10.1136\/jmg.37.8.593"},{"key":"12","doi-asserted-by":"crossref","unstructured":"12. Bruy\u00e8re,              H, Speevak,                MD, Winsor,                EJ, de                Fr\u00e9minville, B,                Farrell,            SA,                McGowan-Jordan,              J, et al.            Isodicentric Yp: prenatal diagnosis and outcome in 12            cases. Prenat Diagn          2006;26: 324\u20139.","DOI":"10.1002\/pd.1406"},{"key":"13","doi-asserted-by":"crossref","unstructured":"13. Saenger,              P, Wikland,                KA, Conway,                GS,                Davenport,              M, Gravholt,                CH, Hintz,                R, et al.            Fifth International Symposium on Turner Syndrome.            Recommendations for the diagnosis and management of Turner            syndrome. 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