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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: moller c. 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.
Localization of Usher syndrome type II to chromosome 1q.
Kimberling WJ, Weston MD, Möller C, Davenport SL, Shugart YY, Priluck IA, Martini A, Milani M, Smith RJ. Kimberling WJ, et al. Among authors: moller c. Genomics. 1990 Jun;7(2):245-9. doi: 10.1016/0888-7543(90)90546-7. Genomics. 1990. PMID: 2347588
Genetic heterogeneity of Usher syndrome type II.
Pieke Dahl S, Kimberling WJ, Gorin MB, Weston MD, Furman JM, Pikus A, Möller C. Pieke Dahl S, et al. Among authors: moller c. J Med Genet. 1993 Oct;30(10):843-8. doi: 10.1136/jmg.30.10.843. J Med Genet. 1993. PMID: 7901420 Free PMC article.
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: moller c. Am J Hum Genet. 1996 Nov;59(5):1074-83. Am J Hum Genet. 1996. PMID: 8900236 Free PMC article.
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: moller c. 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.
770 results