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2. 47,XXX/48,XXXX in a retarded three year old girl with multiple somatic anomalies. Ioan D; Hîrşovescu N; Dumitriu L; Belengeanu V; Muşeţeanu P; Maximilian C Endocrinologie; 1985; 23(2):121-4. PubMed ID: 4035270 [TBL] [Abstract][Full Text] [Related]
3. ["Superfemale syndrome" in a 12-year-old girl (XXXX sex chromosome arrangement) associated with a combination of congenital abnormalities]. Halikowski B; Kleczkowska A; Gościńska Z; Knaus A Pediatr Pol; 1969 Sep; 44(9):1147-54. PubMed ID: 5364501 [No Abstract] [Full Text] [Related]
4. [48, XXXX syndrome in a fourteen year old girl]. Lejeune J; Abonyi D Ann Genet; 1968 Jun; 11(2):117-9. PubMed ID: 5303423 [No Abstract] [Full Text] [Related]
5. [Iridoschisis in a girl with karyotype 48 XXXX]. Hanicka M; Kleczkowska A; Makowska J; Sokolowski J; Jarczyk K Pol Tyg Lek; 1969 Jul; 24(30):1164-6. PubMed ID: 4979871 [No Abstract] [Full Text] [Related]
6. Kabuki syndrome in son and low grade mosaic 45,X/46,XX in mother. Van Hagen JM; Kwee ML; Madan K; Nieuwint AW; Pals G; ten Kate LP Genet Couns; 1996; 7(3):201-6. PubMed ID: 8897041 [TBL] [Abstract][Full Text] [Related]
7. A 48,XXXX female with absence of ovaries. Collen RJ; Falk RE; Lippe BM; Kaplan SA Am J Med Genet; 1980; 6(4):275-8. PubMed ID: 7211945 [TBL] [Abstract][Full Text] [Related]
8. [Syndrome 48,XXXX]. de Grouchy J; Vialatte J; Chavin-Colin F; Roubin M; Turleau C Arch Fr Pediatr; 1979 Nov; 36(9 Suppl):XLI-XLVII. PubMed ID: 539881 [No Abstract] [Full Text] [Related]
9. X-linked syndrome of mental retardation, short stature, and hypertelorism: a new syndrome or a further example of the FG syndrome? Bottani A Am J Med Genet; 1994 May; 51(1):87-8. PubMed ID: 8030678 [No Abstract] [Full Text] [Related]
11. [The triple X syndrome. Apropos of a case]. Lévêque B; Guerineau P Ann Pediatr (Paris); 1965 Nov; 12(11):730-4. PubMed ID: 5853130 [No Abstract] [Full Text] [Related]
12. [49, XXXXX chromosome equipment in a girl with psychophysical underdevelopment]. Giovannucci-Uzielli ML; Torricelli F; Salvatori Q; Consumi I; Donzelli GP; Seminara S Minerva Pediatr; 1975 Dec; 27(40):2220-9. PubMed ID: 1221299 [No Abstract] [Full Text] [Related]
13. Coffin-Lowry syndrome: clinical aspects at different ages and symptoms in female carriers. Plomp AS; De Die-Smulders CE; Meinecke P; Ypma-Verhulst JM; Lissone DA; Fryns JP Genet Couns; 1995; 6(3):259-68. PubMed ID: 8588856 [TBL] [Abstract][Full Text] [Related]
14. Feeblemindedness and XXXX karyotype. Di Cagno L; Franceschini P J Ment Defic Res; 1968 Sep; 12(3):226-36. PubMed ID: 5722467 [No Abstract] [Full Text] [Related]
15. [X chromosome-linked mental retardation with fragile X chromosome and macro-orchidism]. Zollinger A; Schmid W; Vilan J; Sorg B; Knoblauch M Schweiz Med Wochenschr; 1983 Feb; 113(7):238-44. PubMed ID: 6836249 [TBL] [Abstract][Full Text] [Related]
16. Pentasomy X: report of patient and studies of X-inactivation. Funderburk SJ; Valente M; Klisak I Am J Med Genet; 1981; 8(1):27-33. PubMed ID: 7246603 [TBL] [Abstract][Full Text] [Related]
17. X-linked mental retardation, microcephaly, and growth delay associated with hereditary bullous dystrophy macular type: report of a second family. Lungarotti MS; Martello C; Barboni G; Mezzetti D; Mariotti G; Calabro A Am J Med Genet; 1994 Jul; 51(4):598-601. PubMed ID: 7943046 [TBL] [Abstract][Full Text] [Related]
18. [The 48,XXXX syndrome: study of psychomotor development from birth to 11 years of age and review of the literature]. Plauchu H; Ollagnon-Roman E; Armand JP; Robert JM Ann Genet; 1988; 31(2):105-10. PubMed ID: 3041908 [TBL] [Abstract][Full Text] [Related]
19. Kabuki make-up (Niikawa-Kuroki) syndrome with mosaicism ring chromosome X and incomplete XIST gene expression. Su PH; Kuo PL; Chen SJ; Chen JY; Yu JS; Liu YL; Kao IW Acta Paediatr Taiwan; 2007; 48(1):28-31. PubMed ID: 19653414 [TBL] [Abstract][Full Text] [Related]
20. Fragile-X syndrome. A jigsaw puzzle with picture emerging. Townes PL Am J Dis Child; 1982 May; 136(5):389-91. PubMed ID: 7081156 [No Abstract] [Full Text] [Related] [Next] [New Search]