PubMed for id: 339336

Year	Number of Results
1995	3
1996	4
1997	1
1998	3
1999	3
2000	2
2001	4
2002	5
2003	2
2004	2
2005	6
2006	4
2007	2
2008	1
2009	4
2010	3
2011	4
2012	4
2013	3
2014	2
2015	4
2016	4
2017	2
2018	1
2019	3
2020	2
2022	3
2024	0

1

Cone structure in patients with usher syndrome type III and mutations in the Clarin 1 gene.

Ratnam K, Västinsalo H, Roorda A, Sankila EM, Duncan JL. Ratnam K, et al. JAMA Ophthalmol. 2013 Jan;131(1):67-74. doi: 10.1001/2013.jamaophthalmol.2. JAMA Ophthalmol. 2013. PMID: 22964989 Free PMC article.

2

Visual impairment in Finnish Usher syndrome type III.

Plantinga RF, Pennings RJ, Huygen PL, Sankila EM, Tuppurainen K, Kleemola L, Cremers CW, Deutman AF. Plantinga RF, et al. Acta Ophthalmol Scand. 2006 Feb;84(1):36-41. doi: 10.1111/j.1600-0420.2005.00507.x. Acta Ophthalmol Scand. 2006. PMID: 16445437 Free article.

3

Serial audiometry and speech recognition findings in Finnish Usher syndrome type III patients.

Plantinga RF, Kleemola L, Huygen PL, Joensuu T, Sankila EM, Pennings RJ, Cremers CW. Plantinga RF, et al. Audiol Neurootol. 2005 Mar-Apr;10(2):79-89. doi: 10.1159/000083363. Epub 2005 Jan 12. Audiol Neurootol. 2005. PMID: 15650299

4

Usher syndrome type III can mimic other types of Usher syndrome.

Pennings RJ, Fields RR, Huygen PL, Deutman AF, Kimberling WJ, Cremers CW. Pennings RJ, et al. Ann Otol Rhinol Laryngol. 2003 Jun;112(6):525-30. doi: 10.1177/000348940311200608. Ann Otol Rhinol Laryngol. 2003. PMID: 12834121

5

Usher syndrome type III: revised genomic structure of the USH3 gene and identification of novel mutations.

Fields RR, Zhou G, Huang D, Davis JR, Möller C, Jacobson SG, Kimberling WJ, Sumegi J. Fields RR, et al. Am J Hum Genet. 2002 Sep;71(3):607-17. doi: 10.1086/342098. Epub 2002 Jul 16. Am J Hum Genet. 2002. PMID: 12145752 Free PMC article.

6

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

7

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.

8

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

9

The ophthalmological course of Usher syndrome type III.

Pakarinen L, Tuppurainen K, Laippala P, Mäntyjärvi M, Puhakka H. Pakarinen L, et al. Int Ophthalmol. 1995-1996;19(5):307-11. doi: 10.1007/BF00130927. Int Ophthalmol. 1995. PMID: 8864816

10

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

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