Bhattacharya SS - 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: bhattacharya ss. 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: bhattacharya ss. 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. Among authors: bhattacharya ss. 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: bhattacharya ss. 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: bhattacharya ss. 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. Among authors: bhattacharya ss. 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: bhattacharya ss. Genomics. 1991 Dec;11(4):991-6. doi: 10.1016/0888-7543(91)90024-9. Genomics. 1991. PMID: 1783405

8

Association of less common cystic fibrosis mutations with a mild phenotype.

Curtis A, Nelson R, Porteous M, Burn J, Bhattacharya SS. Curtis A, et al. Among authors: bhattacharya ss. J Med Genet. 1991 Jan;28(1):34-7. doi: 10.1136/jmg.28.1.34. J Med Genet. 1991. PMID: 1999830 Free PMC article.

9

Genetic heterogeneity in hereditary haemorrhagic telangiectasia.

Porteous ME, Curtis A, Williams O, Marchuk D, Bhattacharya SS, Burn J. Porteous ME, et al. Among authors: bhattacharya ss. J Med Genet. 1994 Dec;31(12):925-6. doi: 10.1136/jmg.31.12.925. J Med Genet. 1994. PMID: 7891373 Free PMC article.

10

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: bhattacharya ss. Eur J Hum Genet. 1994;2(1):51-8. doi: 10.1159/000472341. Eur J Hum Genet. 1994. PMID: 7913867

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