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6. Fragile X mental retardation syndrome: DNA diagnosis and carrier detection in New Zealand families. Neville L, Cochrane J, Fitzgerald P, Kennedy M. N Z Med J; 1995 Oct 13; 108(1009):404-6. PubMed ID: 7478333 [Abstract] [Full Text] [Related]
10. Linkage and genetic counselling for the fragile X using DNA probes 52A, F9, DX13, and ST14. Mulley JC, Gedeon AK, Thorn KA, Bates LJ, Sutherland GR. Am J Med Genet; 1987 Jun 13; 27(2):435-48. PubMed ID: 2886048 [Abstract] [Full Text] [Related]
14. Fragile X-linked mental retardation and the difficulties of reverse genetics. Jordan BR. Bioessays; 1991 May 13; 13(5):243-51. PubMed ID: 1679986 [Abstract] [Full Text] [Related]
18. A new DNA probe of potential use for diagnosis of the fragile-X syndrome. Lucotte G. Ann Genet; 1990 May 13; 33(2):109-10. PubMed ID: 1978629 [Abstract] [Full Text] [Related]
20. Dilemmas in counselling females with the fragile X syndrome. de Vries BB, van den Boer-van den Berg HM, Niermeijer MF, Tibben A. J Med Genet; 1999 Feb 13; 36(2):167-70. PubMed ID: 10051021 [Abstract] [Full Text] [Related] Page: [Next] [New Search]