Kozman H - Search Results

1

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: kozman h. Genomics. 1991 Sep;11(1):77-82. doi: 10.1016/0888-7543(91)90103-l. Genomics. 1991. PMID: 1684954

2

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: kozman h. 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.

3

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: kozman h. 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.

4

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: kozman h. Am J Hum Genet. 1991 Jun;48(6):1051-7. Am J Hum Genet. 1991. PMID: 2035525 Free PMC article.

5

A linkage map of microsatellite markers on the human X chromosome.

Donnelly A, Kozman H, Gedeon AK, Webb S, Lynch M, Sutherland GR, Richards RI, Mulley JC. Donnelly A, et al. Among authors: kozman h. Genomics. 1994 Apr;20(3):363-70. doi: 10.1006/geno.1994.1189. Genomics. 1994. PMID: 8034308

6

A PCR-based genetic linkage map of human chromosome 16.

Shen Y, Kozman HM, Thompson A, Phillips HA, Holman K, Nancarrow J, Lane S, Chen LZ, Apostolou S, Doggett NA, et al. Shen Y, et al. Among authors: kozman hm. Genomics. 1994 Jul 1;22(1):68-76. doi: 10.1006/geno.1994.1346. Genomics. 1994. PMID: 7959793

7

Fine genetic mapping of the Batten disease locus (CLN3) by haplotype analysis and demonstration of allelic association with chromosome 16p microsatellite loci.

Mitchison HM, Thompson AD, Mulley JC, Kozman HM, Richards RI, Callen DF, Stallings RL, Doggett NA, Attwood J, McKay TR, et al. Mitchison HM, et al. Among authors: kozman hm. Genomics. 1993 May;16(2):455-60. doi: 10.1006/geno.1993.1210. Genomics. 1993. PMID: 8314582

8

Addition of MT, D16S10, D16S4, and D16S91 to the linkage map within 16q12.1-q22.1.

Kozman HM, Gedeon AK, Whitmore S, Suthers GK, Callen DF, Sutherland GR, Mulley JC. Kozman HM, et al. Genomics. 1991 Nov;11(3):756-9. doi: 10.1016/0888-7543(91)90085-s. Genomics. 1991. PMID: 1685482

9

The CEPH consortium linkage map of human chromosome 16.

Kozman HM, Keith TP, Donis-Keller H, White RL, Weissenbach J, Dean M, Vergnaud G, Kidd K, Gusella J, Royle NJ, et al. Kozman HM, et al. Genomics. 1995 Jan 1;25(1):44-58. doi: 10.1016/0888-7543(95)80108-x. Genomics. 1995. PMID: 7774955

10

A (CA)n repeat polymorphism for the human skeletal muscle alpha-actinin gene ACTN2 and its localization on the linkage map of chromosome 1.

Beggs AH, Phillips HA, Kozman H, Mulley JC, Wilton SD, Kunkel LM, Laing NG. Beggs AH, et al. Among authors: kozman h. Genomics. 1992 Aug;13(4):1314-5. doi: 10.1016/0888-7543(92)90054-v. Genomics. 1992. PMID: 1505962

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