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7. Mutation screening of USH3 gene (clarin-1) in Spanish patients with Usher syndrome: low prevalence and phenotypic variability. Aller E; Jaijo T; Oltra S; Alió J; Galán F; Nájera C; Beneyto M; Millán JM Clin Genet; 2004 Dec; 66(6):525-9. PubMed ID: 15521980 [TBL] [Abstract][Full Text] [Related]
8. Prevalence and geographical distribution of Usher syndrome in Germany. Spandau UH; Rohrschneider K Graefes Arch Clin Exp Ophthalmol; 2002 Jun; 240(6):495-8. PubMed ID: 12107518 [TBL] [Abstract][Full Text] [Related]
9. A novel locus for Usher syndrome type II, USH2B, maps to chromosome 3 at p23-24.2. Hmani M; Ghorbel A; Boulila-Elgaied A; Ben Zina Z; Kammoun W; Drira M; Chaabouni M; Petit C; Ayadi H Eur J Hum Genet; 1999 Apr; 7(3):363-7. PubMed ID: 10234513 [TBL] [Abstract][Full Text] [Related]
10. Carriers of the Usher syndrome type IB: is audiometric identification possible? Wagenaar M; Snik AF; Kimberling WJ; Cremers CW Am J Otol; 1996 Nov; 17(6):853-8. PubMed ID: 8915413 [TBL] [Abstract][Full Text] [Related]
11. Early diagnosis of Usher syndrome in children. Mets MB; Young NM; Pass A; Lasky JB Trans Am Ophthalmol Soc; 2000; 98():237-42; discussion 243-5. PubMed ID: 11190026 [TBL] [Abstract][Full Text] [Related]
12. Schizophrenia and mental retardation associated in a pedigree with retinitis pigmentosa and sensorineural deafness. Sharp CW; Muir WJ; Blackwood DH; Walker M; Gosden C; St Clair DM Am J Med Genet; 1994 Dec; 54(4):354-60. PubMed ID: 7726208 [TBL] [Abstract][Full Text] [Related]
13. Identification and in vitro expression of novel CDH23 mutations of patients with Usher syndrome type 1D. von Brederlow B; Bolz H; Janecke A; La O Cabrera A; Rudolph G; Lorenz B; Schwinger E; Gal A Hum Mutat; 2002 Mar; 19(3):268-73. PubMed ID: 11857743 [TBL] [Abstract][Full Text] [Related]
14. Early diagnosis of Usher syndrome in infants and children. Young NM; Mets MB; Hain TC Am J Otol; 1996 Jan; 17(1):30-4. PubMed ID: 8694131 [TBL] [Abstract][Full Text] [Related]
15. A novel locus for Usher syndrome type I, USH1G, maps to chromosome 17q24-25. Mustapha M; Chouery E; Torchard-Pagnez D; Nouaille S; Khrais A; Sayegh FN; Mégarbané A; Loiselet J; Lathrop M; Petit C; Weil D Hum Genet; 2002 Apr; 110(4):348-50. PubMed ID: 11941484 [TBL] [Abstract][Full Text] [Related]
16. Prevalence of 2314delG mutation in Spanish patients with Usher syndrome type II (USH2). Beneyto MM; Cuevas JM; Millán JM; Espinós C; Mateu E; González-Cabo P; Baiget M; Doménech M; Bernal S; Ayuso C; García-Sandoval B; Trujillo MJ; Borrego S; Antiñolo G; Carballo M; Nájera C Ophthalmic Genet; 2000 Jun; 21(2):123-8. PubMed ID: 10916187 [TBL] [Abstract][Full Text] [Related]
17. Clinical findings in obligate carriers of type I Usher syndrome. Wagenaar M; ter Rahe B; van Aarem A; Huygen P; Admiraal R; Bleeker-Wagemakers E; Pinckers A; Kimberling W; Cremers C Am J Med Genet; 1995 Nov; 59(3):375-9. PubMed ID: 8599365 [TBL] [Abstract][Full Text] [Related]
18. [Electrophysiologic tests of the auditory apparatus and vestibular organ in Usher syndrome]. Pośpiech L; Gawron W; Rostkowska-Nadolska B; Koziorowska M Otolaryngol Pol; 2003; 57(1):121-6. PubMed ID: 12741156 [TBL] [Abstract][Full Text] [Related]
19. Clinical and genetic studies in Spanish patients with Usher syndrome type II: description of new mutations and evidence for a lack of genotype--phenotype correlation. Bernal S; Medà C; Solans T; Ayuso C; Garcia-Sandoval B; Valverde D; Del Rio E; Baiget M Clin Genet; 2005 Sep; 68(3):204-14. PubMed ID: 16098008 [TBL] [Abstract][Full Text] [Related]
20. Usher syndrome in four siblings from a consanguineous family of Pakistani origin. Trop I; Schloss MD; Polomeno R; Der Kaloustian V J Otolaryngol; 1995 Apr; 24(2):102-4. PubMed ID: 7602669 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]