Kenyon JB - Search Results

1

Autosomal dominant polycystic kidney disease: localization of the second gene to chromosome 4q13-q23.

Kimberling WJ, Kumar S, Gabow PA, Kenyon JB, Connolly CJ, Somlo S. Kimberling WJ, et al. Among authors: kenyon jb. Genomics. 1993 Dec;18(3):467-72. doi: 10.1016/s0888-7543(11)80001-7. Genomics. 1993. PMID: 8307555

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. 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. Among authors: kenyon jb. Hum Mol Genet. 1992 Oct;1(7):491-5. doi: 10.1093/hmg/1.7.491. Hum Mol Genet. 1992. PMID: 1307249

4

Linkage of Usher syndrome type I gene (USH1B) to the long arm of chromosome 11.

Kimberling WJ, Möller CG, Davenport S, Priluck IA, Beighton PH, Greenberg J, Reardon W, Weston MD, Kenyon JB, Grunkemeyer JA, et al. Kimberling WJ, et al. Among authors: kenyon jb. Genomics. 1992 Dec;14(4):988-94. doi: 10.1016/s0888-7543(05)80121-1. Genomics. 1992. PMID: 1478677

5

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. Among authors: kenyon jb. Hum Genet. 1991 Jun;87(2):129-33. doi: 10.1007/BF00204167. Hum Genet. 1991. PMID: 1676697

6

Linkage heterogeneity of autosomal dominant polycystic kidney disease.

Kimberling WJ, Fain PR, Kenyon JB, Goldgar D, Sujansky E, Gabow PA. Kimberling WJ, et al. Among authors: kenyon jb. N Engl J Med. 1988 Oct 6;319(14):913-8. doi: 10.1056/NEJM198810063191405. N Engl J Med. 1988. PMID: 2843768

7

Genetic studies of Usher syndrome.

Kimberling WJ, Weston MD, Pieke Dahl S, Kenyon JB, Shugart YY, Moller C, Davenport SL, Martini A, Milani M, Smith RJ. Kimberling WJ, et al. Among authors: kenyon jb. Ann N Y Acad Sci. 1991;630:167-75. doi: 10.1111/j.1749-6632.1991.tb19585.x. Ann N Y Acad Sci. 1991. PMID: 1952588 No abstract available.

8

Report on attempts to localize Usher syndrome type 1 by linkage analysis to selected candidate regions.

Pieke Dahl S, Weston MD, Kimberling WJ, Kenyon JB, Shugart YY, Smith RJ. Pieke Dahl S, et al. Among authors: kenyon jb. Ann N Y Acad Sci. 1991;630:298-300. doi: 10.1111/j.1749-6632.1991.tb19612.x. Ann N Y Acad Sci. 1991. PMID: 1952612 No abstract available.

9

Autosomal-dominant, prelingual, nonprogressive sensorineural hearing loss: localization of the gene (DFNA8) to chromosome 11q by linkage in an Austrian family.

Kirschhofer K, Kenyon JB, Hoover DM, Franz P, Weipoltshammer K, Wachtler F, Kimberling WJ. Kirschhofer K, et al. Among authors: kenyon jb. Cytogenet Cell Genet. 1998;82(1-2):126-30. doi: 10.1159/000015086. Cytogenet Cell Genet. 1998. PMID: 9763681

10

Splice-altering variant in COL11A1 as a cause of nonsyndromic hearing loss DFNA37.

Booth KT, Askew JW, Talebizadeh Z, Huygen PLM, Eudy J, Kenyon J, Hoover D, Hildebrand MS, Smith KR, Bahlo M, Kimberling WJ, Smith RJH, Azaiez H, Smith SD. Booth KT, et al. Genet Med. 2019 Apr;21(4):948-954. doi: 10.1038/s41436-018-0285-0. Epub 2018 Sep 24. Genet Med. 2019. PMID: 30245514 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

18 results

Search Page

Filters