Kimberling WJ - Search Results

1

Genetic heterogeneity of Usher syndrome type II: localisation to chromosome 5q.

Pieke-Dahl S, Möller CG, Kelley PM, Astuto LM, Cremers CW, Gorin MB, Kimberling WJ. Pieke-Dahl S, et al. Among authors: kimberling wj. J Med Genet. 2000 Apr;37(4):256-62. doi: 10.1136/jmg.37.4.256. J Med Genet. 2000. PMID: 10745043 Free PMC article.

2

Searching for evidence of DFNB2.

Astuto LM, Kelley PM, Askew JW, Weston MD, Smith RJ, Alswaid AF, Al-Rakaf M, Kimberling WJ. Astuto LM, et al. Among authors: kimberling wj. Am J Med Genet. 2002 May 15;109(4):291-7. doi: 10.1002/ajmg.10384. Am J Med Genet. 2002. PMID: 11992483

3

Genetic heterogeneity of Usher syndrome type II in a Dutch population.

Pieke-Dahl S, van Aarem A, Dobin A, Cremers CW, Kimberling WJ. Pieke-Dahl S, et al. Among authors: kimberling wj. J Med Genet. 1996 Sep;33(9):753-7. doi: 10.1136/jmg.33.9.753. J Med Genet. 1996. PMID: 8880575 Free PMC article.

4

Myosin VIIA mutation screening in 189 Usher syndrome type 1 patients.

Weston MD, Kelley PM, Overbeck LD, Wagenaar M, Orten DJ, Hasson T, Chen ZY, Corey D, Mooseker M, Sumegi J, Cremers C, Moller C, Jacobson SG, Gorin MB, Kimberling WJ. Weston MD, et al. Among authors: kimberling wj. Am J Hum Genet. 1996 Nov;59(5):1074-83. Am J Hum Genet. 1996. PMID: 8900236 Free PMC article.

5

Hearing loss in the RBF/DnJ mouse, a proposed animal model of Usher syndrome type IIa.

Pieke-Dahl S, Ohlemiller KK, McGee J, Walsh EJ, Kimberling WJ. Pieke-Dahl S, et al. Among authors: kimberling wj. Hear Res. 1997 Oct;112(1-2):1-12. doi: 10.1016/s0378-5955(97)00087-7. Hear Res. 1997. PMID: 9367224

6

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. Among authors: kimberling wj. Am J Med Genet. 1998 Apr 13;76(5):395-401. Am J Med Genet. 1998. PMID: 9556298

7

Genomic structure and identification of novel mutations in usherin, the gene responsible for Usher syndrome type IIa.

Weston MD, Eudy JD, Fujita S, Yao S, Usami S, Cremers C, Greenberg J, Ramesar R, Martini A, Moller C, Smith RJ, Sumegi J, Kimberling WJ. Weston MD, et al. Among authors: kimberling wj. Am J Hum Genet. 2000 Apr;66(4):1199-210. doi: 10.1086/302855. Epub 2000 Mar 22. Am J Hum Genet. 2000. PMID: 10729113 Free PMC article.

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. Among authors: kimberling wj. 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

Genetic heterogeneity of Usher syndrome.

Kimberling WJ, Orten D, Pieke-Dahl S. Kimberling WJ, et al. Adv Otorhinolaryngol. 2000;56:11-8. doi: 10.1159/000059077. Adv Otorhinolaryngol. 2000. PMID: 10868209 Review.

10

Genetic heterogeneity of Usher syndrome: analysis of 151 families with Usher type I.

Astuto LM, Weston MD, Carney CA, Hoover DM, Cremers CW, Wagenaar M, Moller C, Smith RJ, Pieke-Dahl S, Greenberg J, Ramesar R, Jacobson SG, Ayuso C, Heckenlively JR, Tamayo M, Gorin MB, Reardon W, Kimberling WJ. Astuto LM, et al. Among authors: kimberling wj. Am J Hum Genet. 2000 Dec;67(6):1569-74. doi: 10.1086/316889. Epub 2000 Nov 1. Am J Hum Genet. 2000. PMID: 11060213 Free PMC article.

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