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2. Double monosomy mosaicism (45,X-45, XX,21-) in a retarded child with multiple congenital malformations. Weber FM; Sparkes RS; Muller H Cytogenetics; 1971; 10(6):404-12. PubMed ID: 5146417 [No Abstract] [Full Text] [Related]
3. 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]
4. Autoradiographic re-appraisal of an XXXxY male as a probable XXXXY with a 4-11 translocation. Ockey CH; De la Chapelle A Cytogenetics; 1967; 6(3):178-92. PubMed ID: 6040472 [No Abstract] [Full Text] [Related]
5. Two human X-autosome translocations identified by autoradiography and fluorescence. Cohen MM; Lin CC; Sybert V; Orecchio EJ Am J Hum Genet; 1972 Sep; 24(5):583-97. PubMed ID: 5054227 [No Abstract] [Full Text] [Related]
6. Chromosomal aberrations in the mildly mentally retarded. Göstason R; Wahlström J; Johannisson T; Holmqvist D J Ment Defic Res; 1991 Jun; 35 ( Pt 3)():240-6. PubMed ID: 1833552 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. Sex chromatin survey among mentally retarded children in Japan. Yanagisawa S; Shuto T J Ment Defic Res; 1970 Sep; 14(3):254-62. PubMed ID: 5518410 [No Abstract] [Full Text] [Related]
9. An extra small metacentric autosome in a mentally retarded boy with multiple malformations. Armendares S; Buentello L; Salamanca F J Med Genet; 1971 Sep; 8(3):378-80. PubMed ID: 5097147 [No Abstract] [Full Text] [Related]
10. Mild intellectual deficits in a child with 49,XXXXY. Hersh JH; Bloom AS; Yen F; Topinka C; Weisskopf B Res Dev Disabil; 1988; 9(2):171-6. PubMed ID: 3406471 [TBL] [Abstract][Full Text] [Related]
11. XY translocation in a boy with ichthyosis, hypogonadism, short stature and mental retardation. Matsumoto T; Taku K; Miike T; Harada N; Niikawa N Clin Genet; 1991 Feb; 39(2):156-8. PubMed ID: 2015697 [No Abstract] [Full Text] [Related]
12. Interstitial deletion in the "critical region" of the long arm of the X chromosome in a mentally retarded boy and his normal mother. Tabor A; Andersen O; Lundsteen C; Niebuhr E; Sardemann H Hum Genet; 1983; 64(2):196-9. PubMed ID: 6885061 [TBL] [Abstract][Full Text] [Related]
13. Cytogenetic studies in a selected group of mentally retarded children. Moghe M; Patel ZM; Peter JJ; Ambani LM Hum Genet; 1981; 58(2):184-7. PubMed ID: 6456981 [TBL] [Abstract][Full Text] [Related]
14. Autosomal translocation in a mentally retarded male child with 46,XY,t(2q-;13q+) complement. Case report and review. Genest P; Lachance R; Poty J; Jacob D J Med Genet; 1971 Dec; 8(4):504-8. PubMed ID: 5149534 [No Abstract] [Full Text] [Related]
15. Unusual X chromosome inactivation in a mentally retarded girl with an interstitial deletion Xq27: implications for the fragile X syndrome. Schmidt M; Certoma A; Du Sart D; Kalitsis P; Leversha M; Fowler K; Sheffield L; Jack I; Danks DM Hum Genet; 1990 Mar; 84(4):347-52. PubMed ID: 2307456 [TBL] [Abstract][Full Text] [Related]
16. An extra small metacentric chromosome in a mentally retarded boy. Ishmael J; Laurence KM J Med Genet; 1968 Dec; 5(4):335-40. PubMed ID: 5713650 [No Abstract] [Full Text] [Related]
17. XXXXY syndrome in a phenotypic male infant with associated cardiac abnormalities. Assemany SR; Neu RL; Gardner LI Humangenetik; 1971; 12(2):101-4. PubMed ID: 5568728 [No Abstract] [Full Text] [Related]
18. Mental retardation in association with a balanced X-autosome translocation and random inactivation of the X chromosomes. Sands ME Clin Genet; 1980 May; 17(5):309-16. PubMed ID: 7438488 [TBL] [Abstract][Full Text] [Related]
19. Phenotype of 49,XXYYY. Das GP; Shukla A; Verma IC Clin Genet; 1993 Apr; 43(4):196-9. PubMed ID: 8330452 [TBL] [Abstract][Full Text] [Related]
20. 49,XXXXY syndrome: behavioural and developmental profiles. Lomelino CA; Reiss AL J Med Genet; 1991 Sep; 28(9):609-12. PubMed ID: 1956059 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]