Holman K - Search Results

1

Fragile X genotype characterized by an unstable region of DNA.

Yu S, Pritchard M, Kremer E, Lynch M, Nancarrow J, Baker E, Holman K, Mulley JC, Warren ST, Schlessinger D, et al. Yu S, et al. Among authors: holman k. Science. 1991 May 24;252(5009):1179-81. doi: 10.1126/science.252.5009.1179. Science. 1991. PMID: 2031189

2

Evidence of founder chromosomes in fragile X syndrome.

Richards RI, Holman K, Friend K, Kremer E, Hillen D, Staples A, Brown WT, Goonewardena P, Tarleton J, Schwartz C, et al. Richards RI, et al. Among authors: holman k. Nat Genet. 1992 Jul;1(4):257-60. doi: 10.1038/ng0792-257. Nat Genet. 1992. PMID: 1302021

3

Characterization of new PCR based markers for mapping and diagnosis: AC dinucleotide repeat markers at the DXS237 (GMGX9) and DXS102 (cX38.1) loci.

Gedeon AK, Holman K, Richards RI, Mulley JC. Gedeon AK, et al. Among authors: holman k. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):255-60. doi: 10.1002/ajmg.1320430140. Am J Med Genet. 1992. PMID: 1351362

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: holman k. Science. 1991 Jun 21;252(5013):1711-4. doi: 10.1126/science.1675488. Science. 1991. PMID: 1675488

5

Dinucleotide repeat polymorphism at D16S287.

Phillips HA, Hyland VJ, Holman K, Callen DF, Richards RI, Mulley JC. Phillips HA, et al. Among authors: holman k. Nucleic Acids Res. 1991 Dec 11;19(23):6664. doi: 10.1093/nar/19.23.6664. Nucleic Acids Res. 1991. PMID: 1754417 Free PMC article. No abstract available.

6

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. Among authors: holman k. 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.

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. Among authors: holman k. Am J Hum Genet. 1991 Jun;48(6):1051-7. Am J Hum Genet. 1991. PMID: 2035525 Free PMC article.

8

A refined physical map of the long arm of human chromosome 16.

Chen LZ, Harris PC, Apostolou S, Baker E, Holman K, Lane SA, Nancarrow JK, Whitmore SA, Stallings RL, Hildebrand CE, et al. Chen LZ, et al. Among authors: holman k. Genomics. 1991 Jun;10(2):308-12. doi: 10.1016/0888-7543(91)90313-4. Genomics. 1991. PMID: 2071140

9

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: holman k. Hum Mol Genet. 1995 Mar;4(3):367-72. doi: 10.1093/hmg/4.3.367. Hum Mol Genet. 1995. PMID: 7795589

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. Among authors: holman k. 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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