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23. Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndrome. Liburd N; Ghosh M; Riazuddin S; Naz S; Khan S; Ahmed Z; Riazuddin S; Liang Y; Menon PS; Smith T; Smith AC; Chen KS; Lupski JR; Wilcox ER; Potocki L; Friedman TB Hum Genet; 2001 Nov; 109(5):535-41. PubMed ID: 11735029 [TBL] [Abstract][Full Text] [Related]
24. [Studies on the genetics and pathology of the development of 8 labyrinth mutants (deaf-waltzer-shaker mutants) in the mouse (Mus musculus)]. KOCHER W Z Vererbungsl; 1960; 91():114-40. PubMed ID: 13853422 [No Abstract] [Full Text] [Related]
25. Gene for topoisomerase III maps within the Smith-Magenis syndrome critical region: analysis of cell-cycle distribution and radiation sensitivity. Elsea SH; Fritz E; Schoener-Scott R; Meyn MS; Patel PI Am J Med Genet; 1998 Jan; 75(1):104-8. PubMed ID: 9450867 [TBL] [Abstract][Full Text] [Related]
26. Chronic strychnine administration into the cochlea potentiates permanent threshold shift following noise exposure. Yamasoba T; Dolan DF Hear Res; 1997 Oct; 112(1-2):13-20. PubMed ID: 9367225 [TBL] [Abstract][Full Text] [Related]
27. Homologous recombination of a flanking repeat gene cluster is a mechanism for a common contiguous gene deletion syndrome. Chen KS; Manian P; Koeuth T; Potocki L; Zhao Q; Chinault AC; Lee CC; Lupski JR Nat Genet; 1997 Oct; 17(2):154-63. PubMed ID: 9326934 [TBL] [Abstract][Full Text] [Related]
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29. Molecular characterization of a genetically unstable region containing the SMS critical area and a breakpoint cluster for human PNETs. Wilgenbus KK; Seranski P; Brown A; Leuchs B; Mincheva A; Lichter P; Poustka A Genomics; 1997 May; 42(1):1-10. PubMed ID: 9177769 [TBL] [Abstract][Full Text] [Related]
30. Genetic and physical delineation of the region of the mouse deafness mutation shaker-2. Wakabayashi Y; Kikkawa Y; Matsumoto Y; Shinbo T; Kosugi S; Chou D; Furuya M; Jishage K; Noda T; Yonekawa H; Kominami R Biochem Biophys Res Commun; 1997 May; 234(1):107-10. PubMed ID: 9168970 [TBL] [Abstract][Full Text] [Related]
31. Genetic mapping of 21 genes on mouse chromosome 11 reveals disruptions in linkage conservation with human chromosome 5. Watkins-Chow DE; Buckwalter MS; Newhouse MM; Lossie AC; Brinkmeier ML; Camper SA Genomics; 1997 Feb; 40(1):114-22. PubMed ID: 9070927 [TBL] [Abstract][Full Text] [Related]
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33. The human inward rectifying K+ channel Kir 2.2 (KCNJ12) gene: gene structure, assignment to chromosome 17p11.1, and identification of a simple tandem repeat polymorphism. Hugnot JP; Pedeutour F; Le Calvez C; Grosgeorge J; Passage E; Fontes M; Lazdunski M Genomics; 1997 Jan; 39(1):113-6. PubMed ID: 9027495 [TBL] [Abstract][Full Text] [Related]
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35. Multi-disciplinary clinical study of Smith-Magenis syndrome (deletion 17p11.2). Greenberg F; Lewis RA; Potocki L; Glaze D; Parke J; Killian J; Murphy MA; Williamson D; Brown F; Dutton R; McCluggage C; Friedman E; Sulek M; Lupski JR Am J Med Genet; 1996 Mar; 62(3):247-54. PubMed ID: 8882782 [TBL] [Abstract][Full Text] [Related]
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