Fragile X syndrome: a unique mutation in man
- PMID: 3545058
- DOI: 10.1146/annurev.ge.20.120186.000545
Fragile X syndrome: a unique mutation in man
Similar articles
-
DNA studies of X-linked mental retardation associated with a fragile site at Xq27.Am J Med Genet. 1986 Jan-Feb;23(1-2):633-42. doi: 10.1002/ajmg.1320230157. Am J Med Genet. 1986. PMID: 3513572 Review.
-
[Familial mental retardation and the fragile X syndrome].Tijdschr Kindergeneeskd. 1984 Feb;52(1):9-15. Tijdschr Kindergeneeskd. 1984. PMID: 6585033 Dutch.
-
The fragile (X) syndrome: the mutation problem.Am J Med Genet. 1986 Jan-Feb;23(1-2):611-7. doi: 10.1002/ajmg.1320230155. Am J Med Genet. 1986. PMID: 3953671
-
Fragile X syndrome.Am J Ment Defic. 1985 Sep;90(2):119-23. Am J Ment Defic. 1985. PMID: 3901755 Review.
-
A counseling guide to the Martin-Bell syndrome.Am J Med Genet. 1987 Jan;26(1):39-44. doi: 10.1002/ajmg.1320260109. Am J Med Genet. 1987. PMID: 3812576 No abstract available.
Cited by
-
Molecular cloning and analysis of the fragile X region in man.Nucleic Acids Res. 1991 May 25;19(10):2567-72. doi: 10.1093/nar/19.10.2567. Nucleic Acids Res. 1991. PMID: 2041732 Free PMC article.
-
New polymorphisms at the DXS98 locus and confirmation of its location proximal to FRAXA by in situ hybridization.Am J Hum Genet. 1989 Feb;44(2):248-54. Am J Hum Genet. 1989. PMID: 2563194 Free PMC article.
-
Physical mapping of DXS134 close to the DXS52 locus.Hum Genet. 1989 Apr;82(1):27-30. doi: 10.1007/BF00288266. Hum Genet. 1989. PMID: 2565864
-
Human Xq24-Xq28: approaches to mapping with yeast artificial chromosomes.Am J Hum Genet. 1990 Jan;46(1):95-106. Am J Hum Genet. 1990. PMID: 2294758 Free PMC article.
-
Interpretation of the heterogeneity in the linkage relationships of DNA markers around the fragile X locus.Hum Genet. 1987 Nov;77(3):297-8. doi: 10.1007/BF00284493. Hum Genet. 1987. PMID: 3479389 No abstract available.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical