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5. Familial autism and the fragile-X chromosome. August GJ, Lockhart LH. J Autism Dev Disord; 1984 Jun; 14(2):197-204. PubMed ID: 6746507 [Abstract] [Full Text] [Related]
6. Deletion of chromosome 2q37 and autism: a distinct subtype? Ghaziuddin M, Burmeister M. J Autism Dev Disord; 1999 Jun; 29(3):259-63. PubMed ID: 10425588 [Abstract] [Full Text] [Related]
8. Prevalence of fra(X) and other specific diagnoses in autistic individuals in a Danish county. Tranebjaerg L, Kure P. Am J Med Genet; 1991 Jun; 38(2-3):212-4. PubMed ID: 2018060 [Abstract] [Full Text] [Related]
11. Chromosomal abnormalities in a series of children with autistic disorder. Konstantareas MM, Homatidis S. J Autism Dev Disord; 1999 Aug; 29(4):275-85. PubMed ID: 10478727 [Abstract] [Full Text] [Related]
16. Chromosome abnormalities in infantile autism and other childhood psychoses: a population study of 66 cases. Gillberg C, Wahlström J. Dev Med Child Neurol; 1985 Jun; 27(3):293-304. PubMed ID: 3160621 [Abstract] [Full Text] [Related]
17. [Neuropediatric approach to autism]. Cuisset JM, Joriot S, Auvin S, Gozé O, Medjkane F, Salloum A, Delion P, Vallée L. Arch Pediatr; 2005 Dec; 12(12):1734-41. PubMed ID: 16219450 [Abstract] [Full Text] [Related]
18. Fragile X and autism: a multicenter survey. Brown WT, Jenkins EC, Cohen IL, Fisch GS, Wolf-Schein EG, Gross A, Waterhouse L, Fein D, Mason-Brothers A, Ritvo E. Am J Med Genet; 1986 Dec; 23(1-2):341-52. PubMed ID: 3513570 [Abstract] [Full Text] [Related]
20. 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] Page: [Next] [New Search]