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Items: 1 to 20 of 250

1.

Chromosomal mapping and phenotypic characterization of hereditary otosclerosis linked to the OTSC4 locus.

Brownstein Z, Goldfarb A, Levi H, Frydman M, Avraham KB.

Arch Otolaryngol Head Neck Surg. 2006 Apr;132(4):416-24.

PMID:
16618911
2.

Localization of a gene for otosclerosis to chromosome 15q25-q26.

Tomek MS, Brown MR, Mani SR, Ramesh A, Srisailapathy CR, Coucke P, Zbar RI, Bell AM, McGuirt WT, Fukushima K, Willems PJ, Van Camp G, Smith RJ.

Hum Mol Genet. 1998 Feb;7(2):285-90.

PMID:
9425236
3.

The genetics of otosclerosis: pedigree studies and linkage analysis.

Saeed SR, Briggs M, Lobo C, Al-Zoubi F, Ramsden RT, Read AP.

Adv Otorhinolaryngol. 2007;65:75-85.

PMID:
17245027
4.

A second gene for otosclerosis, OTSC2, maps to chromosome 7q34-36.

Van Den Bogaert K, Govaerts PJ, Schatteman I, Brown MR, Caethoven G, Offeciers FE, Somers T, Declau F, Coucke P, Van de Heyning P, Smith RJ, Van Camp G.

Am J Hum Genet. 2001 Feb;68(2):495-500. Epub 2001 Jan 16.

5.

The phenotype of the first otosclerosis family linked to OTSC5.

Pauw RJ, De Leenheer EM, Van Den Bogaert K, Huygen PL, Van Camp G, Joosten FB, Cremers CW.

Otol Neurotol. 2006 Apr;27(3):308-15.

PMID:
16639267
6.

A seventh locus for otosclerosis, OTSC7, maps to chromosome 6q13-16.1.

Thys M, Van Den Bogaert K, Iliadou V, Vanderstraeten K, Dieltjens N, Schrauwen I, Chen W, Eleftheriades N, Grigoriadou M, Pauw RJ, Cremers CR, Smith RJ, Petersen MB, Van Camp G.

Eur J Hum Genet. 2007 Mar;15(3):362-8. Epub 2007 Jan 10.

7.

Clinical and genetic analysis of two Tunisian otosclerosis families.

Ali IB, Thys M, Beltaief N, Schrauwen I, Dieltjens N, Vanderstraeten K, Besbes G, Mnif E, Hachicha S, Arab SB, Camp GV.

Am J Med Genet A. 2007 Jul 15;143A(14):1653-60.

PMID:
17568407
8.

No evidence of linkage between 7q33-36 locus (OTSC2) and otosclerosis in seven British Caucasian pedigrees.

Alzoubi FQ, Ollier WR, Ramsden RT, Saeed SR.

J Laryngol Otol. 2007 Dec;121(12):1140-7. Epub 2007 Oct 2.

PMID:
17908356
9.

Monogenic nonsyndromic otosclerosis: audiological and linkage analysis in a large Greek pedigree.

Iliadou V, Van Den Bogaert K, Eleftheriades N, Aperis G, Vanderstraeten K, Fransen E, Thys M, Grigoriadou M, Pampanos A, Economides J, Iliades T, Van Camp G, Petersen MB.

Int J Pediatr Otorhinolaryngol. 2006 Apr;70(4):631-7. Epub 2005 Sep 15.

PMID:
16168495
10.

A Dutch family with hearing loss linked to the DFNA20/26 locus: longitudinal analysis of hearing impairment.

Kemperman MH, De Leenheer EM, Huygen PL, van Wijk E, van Duijnhoven G, Cremers FP, Kremer H, Cremers CW.

Arch Otolaryngol Head Neck Surg. 2004 Mar;130(3):281-8.

PMID:
15023833
11.

Linkage and association studies in a Malaysian family with autosomal recessive non-syndromic hearing loss.

Farah WI, Aminuddin BS, Ruszymah BH.

Malays J Pathol. 2006 Jun;28(1):23-33.

12.

Otosclerosis: a genetically heterogeneous disease involving at least three different genes.

Van Den Bogaert K, Govaerts PJ, De Leenheer EM, Schatteman I, Verstreken M, Chen W, Declau F, Cremers CW, Van De Heyning PH, Offeciers FE, Somers T, Smith RJ, Van Camp G.

Bone. 2002 Apr;30(4):624-30.

PMID:
11934656
13.

Genome-wide linkage scan, fine mapping, and haplotype analysis in a large, inbred, Arab Israeli pedigree suggest a schizophrenia susceptibility locus on chromosome 20p13.

Teltsh O, Kanyas K, Karni O, Levi A, Korner M, Ben-Asher E, Lancet D, Hamdan A, Lerer B, Kohn Y.

Am J Med Genet B Neuropsychiatr Genet. 2008 Mar 5;147B(2):209-15.

PMID:
17823922
14.

A genome-wide scan maps a novel autosomal dominant juvenile-onset open-angle glaucoma locus to 2p15-16.

Lin Y, Liu T, Li J, Yang J, Du Q, Wang J, Yang Y, Liu X, Fan Y, Lu F, Chen Y, Pu Y, Zhang K, He X, Yang Z.

Mol Vis. 2008 Apr 18;14:739-44.

15.

Linkage analysis of high myopia susceptibility locus in 26 families.

Paget S, Julia S, Vitezica ZG, Soler V, Malecaze F, Calvas P.

Mol Vis. 2008;14:2566-74. Epub 2008 Dec 30.

16.

A novel locus for generalized epilepsy with febrile seizures plus in French families.

Baulac S, Gourfinkel-An I, Couarch P, Depienne C, Kaminska A, Dulac O, Baulac M, LeGuern E, Nabbout R.

Arch Neurol. 2008 Jul;65(7):943-51. doi: 10.1001/archneur.65.7.943.

PMID:
18625863
17.

Phenotype-genotype correlations in otosclerosis: clinical features of OTSC2.

Declau F, Van den Bogaert K, Van De Heyning P, Offeciers E, Govaerts P, Van Camp G.

Adv Otorhinolaryngol. 2007;65:114-8.

PMID:
17245031
18.

Susceptibility locus on chromosome 1q23-25 for a schizophrenia subtype resembling deficit schizophrenia identified by latent class analysis.

Holliday EG, McLean DE, Nyholt DR, Mowry BJ.

Arch Gen Psychiatry. 2009 Oct;66(10):1058-67. doi: 10.1001/archgenpsychiatry.2009.136.

PMID:
19805696
19.

Expanded genomewide scan implicates a novel locus at 3q28 among Caribbean hispanics with familial Alzheimer disease.

Lee JH, Cheng R, Santana V, Williamson J, Lantigua R, Medrano M, Arriaga A, Stern Y, Tycko B, Rogaeva E, Wakutani Y, Kawarai T, St George-Hyslop P, Mayeux R.

Arch Neurol. 2006 Nov;63(11):1591-8.

PMID:
17101828
20.

Phenotype description of a Dutch otosclerosis family with suggestive linkage to OTSC7.

Pauw RJ, Huygen PL, Thys M, Van Camp G, Joosten FB, Cremers CW.

Am J Med Genet A. 2007 Jul 15;143A(14):1613-22.

PMID:
17568406

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