Papiha SS - Search Results

1

Linkage to D3S47 (C17) in one large autosomal dominant retinitis pigmentosa family and exclusion in another: confirmation of genetic heterogeneity.

Lester DH, Inglehearn CF, Bashir R, Ackford H, Esakowitz L, Jay M, Bird AC, Wright AF, Papiha SS, Bhattacharya SS. Lester DH, et al. Among authors: papiha ss. Am J Hum Genet. 1990 Sep;47(3):536-41. Am J Hum Genet. 1990. PMID: 2393026 Free PMC article.

2

Linkage of internal minisatellite loci on chromosome 1 and exclusion of autosomal dominant retinitis pigmentosa proximal to rhesus.

Inglehearn CF, Papiha SS, Jay M, Wright AF, Moore AT, Bhattacharya SS. Inglehearn CF, et al. Among authors: papiha ss. J Med Genet. 1990 Jan;27(1):14-6. doi: 10.1136/jmg.27.1.14. J Med Genet. 1990. PMID: 2106582 Free PMC article.

3

No evidence for linkage between late onset autosomal dominant retinitis pigmentosa and chromosome 3 locus D3S47 (C17): evidence for genetic heterogeneity.

Inglehearn CF, Jay M, Lester DH, Bashir R, Jay B, Bird AC, Wright AF, Evans HJ, Papiha SS, Bhattacharya SS. Inglehearn CF, et al. Among authors: papiha ss. Genomics. 1990 Jan;6(1):168-73. doi: 10.1016/0888-7543(90)90462-4. Genomics. 1990. PMID: 2303257

4

X-linked retinitis pigmentosa: a molecular genetic approach to isolating the defective genes.

Lindsay S, Jay M, Bower DJ, Adam G, Inglehearn CF, Sealey PG, Papiha SS, Bhattacharya SS. Lindsay S, et al. Among authors: papiha ss. Prog Clin Biol Res. 1989;314:83-97. Prog Clin Biol Res. 1989. PMID: 2692031 Review. No abstract available.

5

X chromosome restriction fragment length polymorphisms in five racial groups: rare variant detected with the RC8 (DXS9) probe in the Marathi population, India.

Wadhwa R, Papiha S, Lester D, Ray V, Saha N, Bhattacharya S. Wadhwa R, et al. Hum Hered. 1989;39(6):309-12. doi: 10.1159/000153881. Hum Hered. 1989. PMID: 2575595

6

DNA polymorphisms, identified by an X-chromosome short-arm probe L 1.28 (DXS7), in different racial groups.

Papiha SS, Bhattacharya SS, Roberts DF. Papiha SS, et al. Hum Hered. 1988;38(2):72-5. doi: 10.1159/000153761. Hum Hered. 1988. PMID: 2897946

7

Genomic probes in prenatal diagnosis of duchenne muscular dystrophy in Indians and Chinese.

Papiha SS, Bhattacharya SS. Papiha SS, et al. Natl Med J India. 1990 Jan-Feb;3(1):17-19. Natl Med J India. 1990. PMID: 29865128

8

Population frequencies of three DNA alleles linked to the Duchenne muscular dystrophy gene.

Papiha SS, Roberts DF, Clarke A, Burn J, Gardner-Medwin D, Bhattacharya SS. Papiha SS, et al. J Med Genet. 1989 Jun;26(6):390-2. doi: 10.1136/jmg.26.6.390. J Med Genet. 1989. PMID: 2567785 Free PMC article.

9

Variation in DNA polymorphisms of the short arm of the human X chromosome: genetic affinity of Parsi from western India.

al-Maghtheh M, Ray V, Mastana SS, Garralda MD, Bhattacharya SS, Papiha SS. al-Maghtheh M, et al. Among authors: papiha ss. Hum Hered. 1993 Jul-Aug;43(4):239-43. doi: 10.1159/000154137. Hum Hered. 1993. PMID: 8102115

10

Population variation in molecular polymorphisms of the short arm of the human X chromosome.

Papiha SS, Mastana SS, Roberts DF, Onyemelukwe GC, Bhattacharya SS. Papiha SS, et al. Am J Phys Anthropol. 1991 Jul;85(3):329-34. doi: 10.1002/ajpa.1330850312. Am J Phys Anthropol. 1991. PMID: 1680294

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