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4. [The XXXXY syndrome. Report of 7 new cases and review of the literature (author's transl)]. Terheggen HG; Pfeiffer RA; Haug H; Schünke W Z Kinderheilkd; 1973 Oct; 115(3):209-33. PubMed ID: 4203681 [No Abstract] [Full Text] [Related]
5. Epiphysial dysplasia: a constant finding in the XXXXY syndrome. Schmidt R; Pajewski M; Rosenblatt M J Med Genet; 1978 Aug; 15(4):282-7. PubMed ID: 568664 [TBL] [Abstract][Full Text] [Related]
6. 49,XXXXY: a distinct phenotype. Three new cases and review. Peet J; Weaver DD; Vance GH J Med Genet; 1998 May; 35(5):420-4. PubMed ID: 9610808 [TBL] [Abstract][Full Text] [Related]
7. [XXXXY syndrome]. Toudic L; L'Henoret G; Rivière D; L'Hour M; Castel Y Arch Fr Pediatr; 1982 Apr; 39(4):247-9. PubMed ID: 7125819 [TBL] [Abstract][Full Text] [Related]
8. Normal testicular histology in a mid-trimester 49,XXXXY fetus. Fryns JP; Moerman P; Kleczkowska A Clin Genet; 1995 Jun; 47(6):331. PubMed ID: 7554371 [No Abstract] [Full Text] [Related]
9. SRY-negative XX fetus with complete male phenotype. Vilain E; Le Fiblec B; Morichon-Delvallez N; Brauner R; Dommergues M; Dumez Y; Jaubert F; Boucekkine C; McElreavey K; Vekemans M Lancet; 1994 Jan; 343(8891):240-1. PubMed ID: 7904700 [No Abstract] [Full Text] [Related]
10. Prenatal sonographic diagnosis of the 49,XXXXY syndrome. Schluth C; Doray B; Girard-Lemaire F; Kohler M; Langer B; Gasser B; Lindner V; Flori E Prenat Diagn; 2002 Dec; 22(13):1177-80. PubMed ID: 12478628 [TBL] [Abstract][Full Text] [Related]
12. Chromosome banding studies in two patients with XXXXY syndrome. Levy CL; Sparkes RS; Carlson HE J Med Genet; 1978 Aug; 15(4):301-5. PubMed ID: 568665 [TBL] [Abstract][Full Text] [Related]
13. 49, XXXXY syndrome with severe vesico-ureteral reflux and hydronephrosis: report of one case. Chang JT; Chiu PC; Chen YY; Chao MC; Hsieh KS Acta Paediatr Taiwan; 2005; 46(1):35-8. PubMed ID: 16302576 [TBL] [Abstract][Full Text] [Related]
15. The XXXXY chromosome anomaly: report of three new cases and review of 30 cases from the literature. Zaleski WA; Houston CS; Pozsonyi J; Ying KL Can Med Assoc J; 1966 May; 94(22):1143-54. PubMed ID: 4222822 [TBL] [Abstract][Full Text] [Related]
16. [Bone malformations associated with deletion of the long arm of chromosome X]. Hurgoiu V; Suciu S; Nicoară Z; Florescu P; David-Mark S Rev Pediatr Obstet Ginecol Pediatr; 1988; 37(4):373-6. PubMed ID: 3150606 [No Abstract] [Full Text] [Related]
17. 49, XXXXY syndrome in a 1 year-old infant. Molska I; Lech H; Wiśniewski L Klin Padiatr; 1977 Nov; 189(6):477-81. PubMed ID: 563945 [TBL] [Abstract][Full Text] [Related]
18. [A case of neonatal 49,XXXXY syndrome]. Ságodi L; Lukács V; Lechner E Orv Hetil; 1999 Aug; 140(32):1787-90. PubMed ID: 10489762 [TBL] [Abstract][Full Text] [Related]
19. Down's/Turner's mosaicism. Double aneuploidy as a rare cause of missed prenatal diagnosis of chromosomal abnormality. MacFaul R; Turner T; Mason MK Arch Dis Child; 1981 Dec; 56(12):962-3. PubMed ID: 6460476 [TBL] [Abstract][Full Text] [Related]