Holman K - Search Results

1

Dinucleotide repeat polymorphisms at the D16S525, D16S359, D16S531 and D16S522 loci.

Shen Y, Holman K, Doggett NA, Callen DF, Sutherland GR, Richards RI. Shen Y, et al. Among authors: holman k. Hum Mol Genet. 1994 Jan;3(1):210. doi: 10.1093/hmg/3.1.210. Hum Mol Genet. 1994. PMID: 8162034 No abstract available.

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

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: holman k. Hum Mol Genet. 1992 Dec;1(9):773. doi: 10.1093/hmg/1.9.773. Hum Mol Genet. 1992. PMID: 1302615 No abstract available.

4

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

5

Isolation and characterisation of (AC)n microsatellite genetic markers from human chromosome 16.

Thompson AD, Shen Y, Holman K, Sutherland GR, Callen DF, Richards RI. Thompson AD, et al. Among authors: holman k. Genomics. 1992 Jun;13(2):402-8. doi: 10.1016/0888-7543(92)90260-y. Genomics. 1992. PMID: 1612599

6

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

7

Human glandular Kallikrein genes: genetic and physical mapping of the KLK1 locus using a highly polymorphic microsatellite PCR marker.

Richards RI, Holman K, Shen Y, Kozman H, Harley H, Brook D, Shaw D. Richards RI, et al. Among authors: holman k. Genomics. 1991 Sep;11(1):77-82. doi: 10.1016/0888-7543(91)90103-l. Genomics. 1991. PMID: 1684954

8

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.

9

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.

10

Human chromosome 16 physical map: mapping of somatic cell hybrids using multiplex PCR deletion analysis of sequence tagged sites.

Richards RI, Holman K, Lane S, Sutherland GR, Callen DF. Richards RI, et al. Among authors: holman k. Genomics. 1991 Aug;10(4):1047-52. doi: 10.1016/0888-7543(91)90197-m. Genomics. 1991. PMID: 1916811

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