Cremers CW - 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: cremers cw. 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

CDH23 mutation and phenotype heterogeneity: a profile of 107 diverse families with Usher syndrome and nonsyndromic deafness.

Astuto LM, Bork JM, Weston MD, Askew JW, Fields RR, Orten DJ, Ohliger SJ, Riazuddin S, Morell RJ, Khan S, Riazuddin S, Kremer H, van Hauwe P, Moller CG, Cremers CW, Ayuso C, Heckenlively JR, Rohrschneider K, Spandau U, Greenberg J, Ramesar R, Reardon W, Bitoun P, Millan J, Legge R, Friedman TB, Kimberling WJ. Astuto LM, et al. Among authors: cremers cw. Am J Hum Genet. 2002 Aug;71(2):262-75. doi: 10.1086/341558. Epub 2002 Jun 19. Am J Hum Genet. 2002. PMID: 12075507 Free PMC article.

3

Gene mapping of Usher syndrome type IIa: localization of the gene to a 2.1-cM segment on chromosome 1q41.

Kimberling WJ, Weston MD, Möller C, van Aarem A, Cremers CW, Sumegi J, Ing PS, Connolly C, Martini A, Milani M, et al. Kimberling WJ, et al. Among authors: cremers cw. Am J Hum Genet. 1995 Jan;56(1):216-23. Am J Hum Genet. 1995. PMID: 7825581 Free PMC article.

4

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. Among authors: cremers cw. Am J Hum Genet. 1994 Dec;55(6):1188-94. Am J Hum Genet. 1994. PMID: 7977379 Free PMC article.

5

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: cremers cw. 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.

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: cremers cw. Am J Med Genet. 1998 Apr 13;76(5):395-401. Am J Med Genet. 1998. PMID: 9556298

7

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: cremers cw. 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.

8

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: cremers cw. 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.

9

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: cremers cw. Hum Mol Genet. 1992 Oct;1(7):491-5. doi: 10.1093/hmg/1.7.491. Hum Mol Genet. 1992. PMID: 1307249

10

Erratum: analysis of DNA elements that modulate myosin VIIa expression in humans.

Orten DJ, Weston MD, Kelley PM, Cremers CW, Wagenaar M, Jacobson SG, Kimberling WJ. Orten DJ, et al. Among authors: cremers cw. Hum Mutat. 2000 Jan;15(1):114-5. doi: 10.1002/(SICI)1098-1004(200001)15:1<114::AID-HUMU21>3.0.CO;2-4. Hum Mutat. 2000. PMID: 10612833

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