Similar articles for PMID: 8975700

Year	Number of Results
1989	1
1990	4
1991	1
1992	5
1993	1
1994	7
1995	8
1996	10
1997	9
1998	12
1999	7
2000	7
2001	2
2002	7
2003	3
2004	4
2005	3
2006	1
2007	2
2008	1
2010	1
2024	0

1

Refined mapping of the Usher syndrome type III locus on chromosome 3, exclusion of candidate genes, and identification of the putative mouse homologous region.

Joensuu T, Blanco G, Pakarinen L, Sistonen P, Kääriäinen H, Brown S, Chapelle A, Sankila EM. Joensuu T, et al. Genomics. 1996 Dec 15;38(3):255-63. doi: 10.1006/geno.1996.0626. Genomics. 1996. PMID: 8975700

2

A sequence-ready map of the Usher syndrome type III critical region on chromosome 3q.

Joensuu T, Hämäläinen R, Lehesjoki AE, de la Chapelle A, Sankila EM. Joensuu T, et al. Genomics. 2000 Feb 1;63(3):409-16. doi: 10.1006/geno.1999.6096. Genomics. 2000. PMID: 10704288

3

Assignment of an Usher syndrome type III (USH3) gene to chromosome 3q.

Sankila EM, Pakarinen L, Kääriäinen H, Aittomäki K, Karjalainen S, Sistonen P, de la Chapelle A. Sankila EM, et al. Hum Mol Genet. 1995 Jan;4(1):93-8. doi: 10.1093/hmg/4.1.93. Hum Mol Genet. 1995. PMID: 7711740

4

Usher syndrome type III (USH3) linked to chromosome 3q in an Italian family.

Gasparini P, De Fazio A, Croce AI, Stanziale P, Zelante L. Gasparini P, et al. J Med Genet. 1998 Aug;35(8):666-7. doi: 10.1136/jmg.35.8.666. J Med Genet. 1998. PMID: 9719374 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. 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

Mutations in a novel gene with transmembrane domains underlie Usher syndrome type 3.

Joensuu T, Hämäläinen R, Yuan B, Johnson C, Tegelberg S, Gasparini P, Zelante L, Pirvola U, Pakarinen L, Lehesjoki AE, de la Chapelle A, Sankila EM. Joensuu T, et al. Am J Hum Genet. 2001 Oct;69(4):673-84. doi: 10.1086/323610. Epub 2001 Aug 27. Am J Hum Genet. 2001. PMID: 11524702 Free PMC article.

7

Assembly of a high-resolution map of the Acadian Usher syndrome region and localization of the nuclear EF-hand acidic gene.

DeAngelis MM, Doucet JP, Drury S, Sherry ST, Robichaux MB, Den Z, Pelias MZ, Ditta GM, Keats BJ, Deininger PL, Batzer MA. DeAngelis MM, et al. Biochim Biophys Acta. 1998 Jul 1;1407(1):84-91. doi: 10.1016/s0925-4439(98)00025-8. Biochim Biophys Acta. 1998. PMID: 9639681 Free article.

8

[From gene to disease; genetic causes of hearing loss and visual impairment sometimes accompanied by vestibular problems (Usher syndrome)].

Pennings RJ, Kremer H, Deutman AF, Kimberling WJ, Cremers CW. Pennings RJ, et al. Ned Tijdschr Geneeskd. 2002 Dec 7;146(49):2354-8. Ned Tijdschr Geneeskd. 2002. PMID: 12510399 Review. Dutch.

9

Clinical and genetic linkage analysis of a large Venezuelan kindred with Usher syndrome.

Keogh IJ, Godinho RN, Wu TP, Diaz de Palacios AM, Palacios N, Bello de Alford M, De Almada MI, MarPalacios N, Vazquez A, Mattei R, Seidman C, Seidman J, Eavey RD. Keogh IJ, et al. Int J Pediatr Otorhinolaryngol. 2004 Aug;68(8):1063-8. doi: 10.1016/j.ijporl.2004.04.005. Int J Pediatr Otorhinolaryngol. 2004. PMID: 15236894

10

Linkage analysis in Usher syndrome type I (USH1) families from Spain.

Espinós C, Nájera C, Millán JM, Ayuso C, Baiget M, Pérez-Garrigues H, Rodrigo O, Vilela C, Beneyto M. Espinós C, et al. J Med Genet. 1998 May;35(5):391-8. doi: 10.1136/jmg.35.5.391. J Med Genet. 1998. PMID: 9610802 Free PMC article.

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