Home > Node > Subnode A boy with karotype 49, XXXXY Zizka, J.; Balícek, P.; Jüttnerová, V.; Semecký, V. Ceskoslovenska Pediatrie 33(1): 20-231978ISSN/ISBN: 0069-2328 PMID: 657337 Document Number: 133290 Document emailed within 1 workday Purchase for $29.90 Secure & encrypted paymentsRelated DocumentsDar, H.; Keynan, A.; Eides, E. 1972: Congenital malformations in an infant with triple x karotype Harefuah 83(6): 243-244Boon, W.H.; Seng, C.T. 1970: A Chinese infant with XXXXY sex chromosomes Journal of the Singapore Paediatric Society 12(1): 52-57Garau, A.; Crisponi, G.G.; Floris, G.; Lucia, G. 1974: Case of polysomy X with 49 chromosomes (syndrome 49 XXXXY) Minerva Pediatrica 26(25): 1249-1259Tumba, A. 1974: Biometric examination of XXXXY subjects, their parents, and their siblings L'Union Medicale du Canada 103(10): 1729-1735Boyd, J.H.; Buchin, S.Y. 1976: The chromosome 49, XXXXY syndrome: report of a case in an adult Arizona Medicine 33(7): 546-550Simşek, P.O.; Utine, G.ül.E.; Alikaşifoğlu, A.; Alanay, Y.; Boduroğlu, K.; Kandemir, N.ün. 2009: Rare sex chromosome aneuploidies: 49,XXXXY and 48,XXXY syndromes Turkish Journal of Pediatrics 51(3): 294-297Colmant, A.; David, T.; Bertheas, M.F.; Fraisse, J.; Freycon, F. 1985: A case of 49 XXXXY gonadosomatic dysgenesis: clinical elements and biological consequences of polysomy X Pediatrie 40(7): 565-571Yildirim, M.S.; Elmas, S.; Baysal, T.; Dogan, M.; Karaaslan, S. 2006: Patent ductus arteriosus, ventricular septal defect and pulmonary hypertension in a child with 49, XXXXY syndrome Genetic Counseling 17(3): 391-393