Lindsay S - Search Results

1

The gene for Aarskog syndrome is located between DXS255 and DXS566 (Xp11.2-Xq13).

Porteous ME, Curtis A, Lindsay S, Williams O, Goudie D, Kamakari S, Bhattacharya SS. Porteous ME, et al. Among authors: lindsay s. Genomics. 1992 Oct;14(2):298-301. doi: 10.1016/s0888-7543(05)80219-8. Genomics. 1992. PMID: 1427846

2

Genetic and physical mapping of five novel microsatellite markers on human Xp21.1-p11.22.

Thiselton DL, Lindsay S, Kamakari S, Hardcastle AJ, Roustan P, Bhattacharya SS. Thiselton DL, et al. Among authors: lindsay s. Genomics. 1995 Jan 1;25(1):279-81. doi: 10.1016/0888-7543(95)80136-a. Genomics. 1995. PMID: 7774929

3

Isolation and characterization of three microsatellite markers in the proximal long arm of the human X chromosome.

Lindsay S, Curtis AR, Roustan P, Kamakari S, Thiselton DL, Stephenson A, Bhattacharya SS. Lindsay S, et al. Genomics. 1993 Jul;17(1):208-10. doi: 10.1006/geno.1993.1303. Genomics. 1993. PMID: 8406451

4

Two dinucleotide repeat polymorphisms at the DXS571 locus.

Curtis AR, Roustan P, Kamakari S, Thiselton D, Lindsay S, Bhattacharya SS. Curtis AR, et al. Among authors: lindsay s. Hum Mol Genet. 1992 Dec;1(9):776. doi: 10.1093/hmg/1.9.776. Hum Mol Genet. 1992. PMID: 1302618 No abstract available.

5

Dinucleotide repeat polymorphism at the DXS559 locus.

Roustan P, Curtis AR, Kamakari S, Thiselton D, Lindsay S, Bhattacharya SS. Roustan P, et al. Among authors: lindsay s. Hum Mol Genet. 1992 Dec;1(9):778. doi: 10.1093/hmg/1.9.778. Hum Mol Genet. 1992. PMID: 1302620 No abstract available.

6

Localisation of the gene for Norrie disease to between DXS7 and DXS426 on Xp.

Lindsay S, Thiselton DL, Bateman JB, Ngo JT, Sparkes RS, Coleman M, Davies KE, Bhattacharya SS. Lindsay S, et al. Hum Genet. 1992 Jan;88(3):349-50. doi: 10.1007/BF00197273. Hum Genet. 1992. PMID: 1733838

7

Genetic and physical mapping around the properdin P gene.

Coleman MP, Murray JC, Willard HF, Nolan KF, Reid KB, Blake DJ, Lindsay S, Bhattacharya SS, Wright A, Davies KE. Coleman MP, et al. Among authors: lindsay s. Genomics. 1991 Dec;11(4):991-6. doi: 10.1016/0888-7543(91)90024-9. Genomics. 1991. PMID: 1783405

8

FISH mapping of 22 novel X chromosome cosmids and the isolation of a novel microsatellite on proximal Xp.

Kamakari S, Thiselton D, Lindsay S, Hardcastle A, Bhattacharya S. Kamakari S, et al. Among authors: lindsay s. Cytogenet Cell Genet. 1995;71(2):151-4. doi: 10.1159/000134096. Cytogenet Cell Genet. 1995. PMID: 7656586

9

A study of X chromosome activity in two incontinentia pigmenti families with probable linkage to Xq28.

Curtis AR, Lindsay S, Boye E, Clarke AJ, Landy SJ, Bhattacharya SS. Curtis AR, et al. Among authors: lindsay s. Eur J Hum Genet. 1994;2(1):51-8. doi: 10.1159/000472341. Eur J Hum Genet. 1994. PMID: 7913867

10

X chromosome linkage studies in familial Rett syndrome.

Curtis AR, Headland S, Lindsay S, Thomas NS, Boye E, Kamakari S, Roustan P, Anvret M, Wahlstrom J, McCarthy G, et al. Curtis AR, et al. Among authors: lindsay s. Hum Genet. 1993 Jan;90(5):551-5. doi: 10.1007/BF00217457. Hum Genet. 1993. PMID: 8094068

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