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Journal Abstract Search
143 related items for PubMed ID: 3334020
1. Fragile X syndrome in Japanese patients with infantile autism. Matsuishi T, Shiotsuki Y, Niikawa N, Katafuchi Y, Otaki E, Ando H, Yamashita Y, Horikawa M, Urabe F, Kuriya N. Pediatr Neurol; 1987; 3(5):284-7. PubMed ID: 3334020 [Abstract] [Full Text] [Related]
8. Infantile autism: an occasional manifestation of fragile (X) mental retardation. McGillivray BC, Herbst DS, Dill FJ, Sandercock HJ, Tischler B. Am J Med Genet; 1986; 23(1-2):353-8. PubMed ID: 3953653 [Abstract] [Full Text] [Related]
9. Cytogenetic survey for autistic fragile X carriers in a mental retardation center. Cantú ES, Stone JW, Wing AA, Langee HR, Williams CA. Am J Ment Retard; 1990 Jan; 94(4):442-7. PubMed ID: 2297426 [Abstract] [Full Text] [Related]
10. Fragile X-chromosome among child psychiatric patients with disturbances of language and social relationships. A pilot study. Jørgensen OS, Nielsen KB, Isager T, Mouridsen SE. Acta Psychiatr Scand; 1984 Nov; 70(5):510-4. PubMed ID: 6516896 [Abstract] [Full Text] [Related]
12. [Fragile X chromosome in autism and psychotic disorders in children]. Bursztejn C, Alembik Y, Stoll C, Poupier G, Feller L, Hamon J, Tribout JL, Gardone MC, Danion-Grilliat A. Arch Fr Pediatr; 1992 Feb; 49(2):99-103. PubMed ID: 1580745 [Abstract] [Full Text] [Related]
13. Autism is not associated with the fragile X syndrome. Einfeld S, Molony H, Hall W. Am J Med Genet; 1989 Oct; 34(2):187-93. PubMed ID: 2816996 [Abstract] [Full Text] [Related]
15. Autism and the fragile X syndrome. Fisch GS, Cohen IL, Wolf EG, Brown WT, Jenkins EC, Gross A. Am J Psychiatry; 1986 Jan; 143(1):71-3. PubMed ID: 3455802 [Abstract] [Full Text] [Related]
17. Frequency of the fragile X syndrome in Japanese mentally retarded males. Arinami T, Kondo I, Nakajima S. Hum Genet; 1986 Aug; 73(4):309-12. PubMed ID: 3744362 [Abstract] [Full Text] [Related]
18. Fragile X syndrome associated with Tourette symptomatology in a male with moderate mental retardation and autism. Kerbeshian J, Burd L, Martsolf JT. J Dev Behav Pediatr; 1984 Aug; 5(4):201-3. PubMed ID: 6590572 [No Abstract] [Full Text] [Related]
20. A "new" chromosome marker common to the Rett syndrome and infantile autism? The frequency of fragile sites at X p22 in 81 children with infantile autism, childhood psychosis and the Rett syndrome. Gillberg C, Wahlström J, Hagberg B. Brain Dev; 1985 Aug; 7(3):365-7. PubMed ID: 3864386 [Abstract] [Full Text] [Related] Page: [Next] [New Search]