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References
- Archidiacono N, Rochi M, Filippi G. 1979. X pentasomy: a case and review. Human Genetics 52: 69–77.
- Carpenter DG, Connolly JM, Carter CH, Kanarek KS. 1979. The penta X (49, xxxxx) syndrome: danger of confusing phenotype with mongolism. American Journal of Diseases of Children 133:330.
- Funderburk SJ, Valente M, Klisak I. 1981. Pentasomy X: report of patient and studies of x-inactivation. American Journal of Medical Genetics 8:27 — 33.
- Kassai R, Hamanda I, Furyta H, Cho K, Abe K, Deng HX. 1991. PentaX Syndrome: A case report with review of the literature. American Journal of Medical Genetics 40:51–56.
- Leal CA, Belmont JW, Nachtman R, Cantu JM, Medina C. 1994. Parental origin of the extra chromosome in polysomy X. Human Genetics 94: 423–6.
- Martini G, Carillo G, Catizone F, Notarangelo A, Mingarelli R, Dallapiccola B. 1993. On the prenatal origin of the X's in a prenatally diagnosed 49, xxxxx syndrome. Prenatal Diagnosis 13:763–6.
- Myles TD, Burd L, Font G, McCorquodale MM, McCorquodale DJ. 1995. Dandy-Walker malformation in a fetus with pentas-omy X (49 xxxxx) prenatally diagnosed by fluorescence in situ hybridisation technique. Fetal Diagnosis Theory 10:333-336. Rooney DE. 2001. Human cytogenetics, constitutional analysis. 3rd ed. Oxford: Oxford University Press.