108 related articles for article (PubMed ID: 2562904)
21. Identification of candidate regions for a novel Usher syndrome type II locus.
Ben Rebeh I; Benzina Z; Dhouib H; Hadjamor I; Amyere M; Ayadi L; Turki K; Hammami B; Kmiha N; Kammoun H; Hakim B; Charfedine I; Vikkula M; Ghorbel A; Ayadi H; Masmoudi S
Mol Vis; 2008 Sep; 14():1719-26. PubMed ID: 18806881
[TBL] [Abstract][Full Text] [Related]
22. A DNA linkage study of Usher's syndrome excluding much of chromosome 4.
Smith RJ
Laryngoscope; 1989 Sep; 99(9):940-9. PubMed ID: 2770384
[TBL] [Abstract][Full Text] [Related]
23. Gene mapping of the Usher syndromes.
Kimberling W; Smith RJ
Otolaryngol Clin North Am; 1992 Oct; 25(5):923-34. PubMed ID: 1408196
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. Volumetric neuroimaging in Usher syndrome: evidence of global involvement.
Schaefer GB; Bodensteiner JB; Thompson JN; Kimberling WJ; Craft JM
Am J Med Genet; 1998 Aug; 79(1):1-4. PubMed ID: 9738858
[TBL] [Abstract][Full Text] [Related]
26. 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]
27. Longterm visual prognosis in Usher syndrome types 1 and 2.
Sadeghi AM; Eriksson K; Kimberling WJ; Sjöström A; Möller C
Acta Ophthalmol Scand; 2006 Aug; 84(4):537-44. PubMed ID: 16879578
[TBL] [Abstract][Full Text] [Related]
28. Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Weil D; Blanchard S; Kaplan J; Guilford P; Gibson F; Walsh J; Mburu P; Varela A; Levilliers J; Weston MD
Nature; 1995 Mar; 374(6517):60-1. PubMed ID: 7870171
[TBL] [Abstract][Full Text] [Related]
29. The spectrum of "complicated spastic paraplegia, MASA syndrome and X-linked hydrocephalus". Contribution of DNA linkage analysis in genetic counseling of individual families.
Schrander-Stumpel C; Meyer H; Merckx D; Jones M; Israel J; Sommer A; Stevens C; Tinschert S; Wilson G; Willems P
Genet Couns; 1994; 5(1):1-10. PubMed ID: 8031529
[TBL] [Abstract][Full Text] [Related]
30. Pigmentary retinopathy, hearing loss, mental retardation, and dysmorphism in sibs: a new syndrome?
Hersh JH; Podruch PE; Weisskopf B
Birth Defects Orig Artic Ser; 1982; 18(3B):175-82. PubMed ID: 7139098
[No Abstract] [Full Text] [Related]
31. 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]
32. Usher syndrome type III can mimic other types of Usher syndrome.
Pennings RJ; Fields RR; Huygen PL; Deutman AF; Kimberling WJ; Cremers CW
Ann Otol Rhinol Laryngol; 2003 Jun; 112(6):525-30. PubMed ID: 12834121
[TBL] [Abstract][Full Text] [Related]
33. Identification of a new mutation of the myosin VII head region in Usher syndrome type 1.
Liu XZ; Newton VE; Steel KP; Brown SD
Hum Mutat; 1997; 10(2):168-70. PubMed ID: 9259201
[No Abstract] [Full Text] [Related]
34. [Perform vestibular test among all small deaf children! Early detection of Usher syndrome improves the possibilities of communication in the event of later deaf-blindness].
Konrádsson K; Magnusson M; Andréasson S
Lakartidningen; 1998 Jan; 95(5):379-81. PubMed ID: 9492482
[TBL] [Abstract][Full Text] [Related]
35. A new clinical classification for Usher's syndrome based on a new subtype of Usher's syndrome type I.
Otterstedde CR; Spandau U; Blankenagel A; Kimberling WJ; Reisser C
Laryngoscope; 2001 Jan; 111(1):84-6. PubMed ID: 11192904
[TBL] [Abstract][Full Text] [Related]
36. 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
J Med Genet; 2000 Apr; 37(4):256-62. PubMed ID: 10745043
[TBL] [Abstract][Full Text] [Related]
37. Fine mapping of the usher syndrome type IC to chromosome 11p14 and identification of flanking markers by haplotype analysis.
Ayyagari R; Li Y; Smith RJ; Pelias MZ; Hejtmancik JF
Mol Vis; 1995 Oct; 1():2. PubMed ID: 9238080
[TBL] [Abstract][Full Text] [Related]
38. Presumed drusen of optic nerve head in siblings with Usher syndrome.
Shiono T; Noro M; Tamai M
Jpn J Ophthalmol; 1991; 35(3):300-5. PubMed ID: 1770670
[TBL] [Abstract][Full Text] [Related]
39. Usher syndrome in four Norwegian counties.
Grøndahl J; Mjøen S
Clin Genet; 1986 Jul; 30(1):14-28. PubMed ID: 3757293
[TBL] [Abstract][Full Text] [Related]
40. 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
Genomics; 1990 Jun; 7(2):245-9. PubMed ID: 2347588
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
