Kumar S - Search Results

1

Refined localization of the branchiootorenal syndrome gene by linkage and haplotype analysis.

Ni L, Wagner MJ, Kimberling WJ, Pembrey ME, Grundfast KM, Kumar S, Daiger SP, Wells DE, Johnson K, Smith RJ. Ni L, et al. Among authors: kumar s. Am J Med Genet. 1994 Jun 1;51(2):176-84. doi: 10.1002/ajmg.1320510222. Am J Med Genet. 1994. PMID: 8092199

2

Localization of the gene for branchiootorenal syndrome to chromosome 8q.

Smith RJ, Coppage KB, Ankerstjerne JK, Capper DT, Kumar S, Kenyon J, Tinley S, Comeau K, Kimberling WJ. Smith RJ, et al. Among authors: kumar s. Genomics. 1992 Dec;14(4):841-4. doi: 10.1016/s0888-7543(05)80102-8. Genomics. 1992. PMID: 1478663

3

Autosomal dominant branchio-oto-renal syndrome--localization of a disease gene to chromosome 8q by linkage in a Dutch family.

Kumar S, Kimberling WJ, Kenyon JB, Smith RJ, Marres HA, Cremers CW. Kumar S, et al. Hum Mol Genet. 1992 Oct;1(7):491-5. doi: 10.1093/hmg/1.7.491. Hum Mol Genet. 1992. PMID: 1307249

4

Genetic linkage studies of autosomal dominant polycystic kidney disease: search for the second gene in a large Sicilian family.

Kumar S, Kimberling WJ, Gabow PA, Kenyon JB. Kumar S, et al. Hum Genet. 1991 Jun;87(2):129-33. doi: 10.1007/BF00204167. Hum Genet. 1991. PMID: 1676697

5

Exclusion of autosomal dominant polycystic kidney disease type II (ADPKD2) from 160 cM of chromosome 1.

Kumar S, Kimberling WJ, Gabow PA, Shugart YY, Pieke-Dahl S. Kumar S, et al. J Med Genet. 1990 Nov;27(11):697-700. doi: 10.1136/jmg.27.11.697. J Med Genet. 1990. PMID: 1980516 Free PMC article.

6

Refining the region of branchio-oto-renal syndrome and defining the flanking markers on chromosome 8q by genetic mapping.

Kumar S, Kimberling WJ, Connolly CJ, Tinley S, Marres HA, Cremers CW. Kumar S, et al. Am J Hum Genet. 1994 Dec;55(6):1188-94. Am J Hum Genet. 1994. PMID: 7977379 Free PMC article.

7

Autosomal-dominant branchio-otic (BO) syndrome is not allelic to the branchio-oto-renal (BOR) gene at 8q13.

Kumar S, Marres HA, Cremers CW, Kimberling WJ. Kumar S, et al. Am J Med Genet. 1998 Apr 13;76(5):395-401. Am J Med Genet. 1998. PMID: 9556298

8

Genomewide search and genetic localization of a second gene associated with autosomal dominant branchio-oto-renal syndrome: clinical and genetic implications.

Kumar S, Deffenbacher K, Marres HA, Cremers CW, Kimberling WJ. Kumar S, et al. Am J Hum Genet. 2000 May;66(5):1715-20. doi: 10.1086/302890. Epub 2000 Apr 3. Am J Hum Genet. 2000. PMID: 10762556 Free PMC article.

9

The genetics of cystic diseases of the kidney.

Kimberling WJ, Pieke-Dahl SA, Kumar S. Kimberling WJ, et al. Among authors: kumar s. Semin Nephrol. 1991 Nov;11(6):596-606. Semin Nephrol. 1991. PMID: 1767134 Review. No abstract available.

10

Genetic heterogeneity associated with branchio-oto-renal syndrome.

Kumar S, Kimberling WJ, Marres HA, Cremers CW. Kumar S, et al. Am J Med Genet. 1999 Mar 19;83(3):207-8. doi: 10.1002/(sici)1096-8628(19990319)83:3<207::aid-ajmg12>3.0.co;2-a. Am J Med Genet. 1999. PMID: 10096598 No abstract available.

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