Richards RI - Search Results

1

Molecular basis of p(CCG)n repeat instability at the FRA16A fragile site locus.

Nancarrow JK, Holman K, Mangelsdorf M, Hori T, Denton M, Sutherland GR, Richards RI. Nancarrow JK, et al. Among authors: richards ri. Hum Mol Genet. 1995 Mar;4(3):367-72. doi: 10.1093/hmg/4.3.367. Hum Mol Genet. 1995. PMID: 7795589

2

Four dinucleotide repeat polymorphisms on human chromosome 16 at D16S289, D16S318, D16S319 and D16S320.

Shen Y, Thompson AT, Holman K, Callen DF, Sutherland GR, Richards RI. Shen Y, et al. Among authors: richards ri. Hum Mol Genet. 1992 Dec;1(9):773. doi: 10.1093/hmg/1.9.773. Hum Mol Genet. 1992. PMID: 1302615 No abstract available.

3

Experience with direct molecular diagnosis of fragile X.

Mulley JC, Yu S, Gedeon AK, Donnelly A, Turner G, Loesch D, Chapman CJ, Gardner RJ, Richards RI, Sutherland GR. Mulley JC, et al. Among authors: richards ri. J Med Genet. 1992 Jun;29(6):368-74. doi: 10.1136/jmg.29.6.368. J Med Genet. 1992. PMID: 1619631 Free PMC article.

4

Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n.

Kremer EJ, Pritchard M, Lynch M, Yu S, Holman K, Baker E, Warren ST, Schlessinger D, Sutherland GR, Richards RI. Kremer EJ, et al. Among authors: richards ri. Science. 1991 Jun 21;252(5013):1711-4. doi: 10.1126/science.1675488. Science. 1991. PMID: 1675488

5

Fragile X syndrome: genetic localisation by linkage mapping of two microsatellite repeats FRAXAC1 and FRAXAC2 which immediately flank the fragile site.

Richards RI, Holman K, Kozman H, Kremer E, Lynch M, Pritchard M, Yu S, Mulley J, Sutherland GR. Richards RI, et al. J Med Genet. 1991 Dec;28(12):818-23. doi: 10.1136/jmg.28.12.818. J Med Genet. 1991. PMID: 1757956 Free PMC article.

6

Dinucleotide repeat polymorphism at the D16S288 locus.

Shen Y, Holman K, Thompson A, Kozman H, Callen DF, Sutherland GR, Richards RI. Shen Y, et al. Among authors: richards ri. Nucleic Acids Res. 1991 Oct 11;19(19):5445. doi: 10.1093/nar/19.19.5445. Nucleic Acids Res. 1991. PMID: 1923835 Free PMC article. No abstract available.

7

Fragile X syndrome: diagnosis using highly polymorphic microsatellite markers.

Richards RI, Shen Y, Holman K, Kozman H, Hyland VJ, Mulley JC, Sutherland GR. Richards RI, et al. Am J Hum Genet. 1991 Jun;48(6):1051-7. Am J Hum Genet. 1991. PMID: 2035525 Free PMC article.

8

The molecular basis of fragile sites in human chromosomes.

Sutherland GR, Richards RI. Sutherland GR, et al. Among authors: richards ri. Curr Opin Genet Dev. 1995 Jun;5(3):323-7. doi: 10.1016/0959-437x(95)80046-8. Curr Opin Genet Dev. 1995. PMID: 7549426 Review.

9

Simple tandem DNA repeats and human genetic disease.

Sutherland GR, Richards RI. Sutherland GR, et al. Among authors: richards ri. Proc Natl Acad Sci U S A. 1995 Apr 25;92(9):3636-41. doi: 10.1073/pnas.92.9.3636. Proc Natl Acad Sci U S A. 1995. PMID: 7731957 Free PMC article. Review.

10

Haplotype analysis at the FRAXA locus in the Japanese population.

Richards RI, Kondo I, Holman K, Yamauchi M, Seki N, Kishi K, Staples A, Sutherland GR, Hori T. Richards RI, et al. Am J Med Genet. 1994 Jul 15;51(4):412-6. doi: 10.1002/ajmg.1320510422. Am J Med Genet. 1994. PMID: 7943009

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