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Items: 1 to 20 of 108

1.

Autosomal recessive nonsyndromic deafness locus DFNB63 at chromosome 11q13.2-q13.3.

Khan SY, Riazuddin S, Tariq M, Anwar S, Shabbir MI, Riazuddin SA, Khan SN, Husnain T, Ahmed ZM, Friedman TB, Riazuddin S.

Hum Genet. 2007 Feb;120(6):789-93. Epub 2006 Oct 26.

PMID:
17066295
2.

A novel locus for autosomal recessive nonsyndromic hearing impairment, DFNB63, maps to chromosome 11q13.2-q13.4.

Kalay E, Caylan R, Kiroglu AF, Yasar T, Collin RW, Heister JG, Oostrik J, Cremers CW, Brunner HG, Karaguzel A, Kremer H.

J Mol Med (Berl). 2007 Apr;85(4):397-404. Epub 2007 Jan 9.

PMID:
17211611
3.

Localization of a novel autosomal recessive non-syndromic hearing impairment locus DFNB63 to chromosome 11q13.3-q13.4.

Tlili A, Masmoudi S, Dhouib H, Bouaziz S, Rebeh IB, Chouchen J, Turki K, Benzina Z, Charfedine I, Drira M, Ayadi H.

Ann Hum Genet. 2007 Mar;71(Pt 2):271-5. Epub 2006 Dec 12.

4.

DFNB39, a recessive form of sensorineural hearing impairment, maps to chromosome 7q11.22-q21.12.

Wajid M, Abbasi AA, Ansar M, Pham TL, Yan K, Haque S, Ahmad W, Leal SM.

Eur J Hum Genet. 2003 Oct;11(10):812-5.

5.

A novel autosomal recessive non-syndromic deafness locus (DFNB35) maps to 14q24.1-14q24.3 in large consanguineous kindred from Pakistan.

Ansar M, Din MA, Arshad M, Sohail M, Faiyaz-Ul-Haque M, Haque S, Ahmad W, Leal SM.

Eur J Hum Genet. 2003 Jan;11(1):77-80.

6.

A novel locus DFNA59 for autosomal dominant nonsyndromic hearing loss maps at chromosome 11p14.2-q12.3.

Chatterjee A, Jalvi R, Pandey N, Rangasayee R, Anand A.

Hum Genet. 2009 Jan;124(6):669-75. doi: 10.1007/s00439-008-0596-3. Epub 2008 Nov 22.

PMID:
19030898
7.

The autosomal recessive nonsyndromic deafness locus DFNB72 is located on chromosome 19p13.3.

Ain Q, Nazli S, Riazuddin S, Jaleel AU, Riazuddin SA, Zafar AU, Khan SN, Husnain T, Griffith AJ, Ahmed ZM, Friedman TB, Riazuddin S.

Hum Genet. 2007 Dec;122(5):445-50. Epub 2007 Aug 10.

PMID:
17690910
8.
9.

DFNB31, a recessive form of sensorineural hearing loss, maps to chromosome 9q32-34.

Mustapha M, Chouery E, Chardenoux S, Naboulsi M, Paronnaud J, Lemainque A, Mégarbané A, Loiselet J, Weil D, Lathrop M, Petit C.

Eur J Hum Genet. 2002 Mar;10(3):210-2.

10.

The mapping of DFNB62, a new locus for autosomal recessive non-syndromic hearing impairment, to chromosome 12p13.2-p11.23.

Ali G, Santos RL, John P, Wambangco MA, Lee K, Ahmad W, Leal S.

Clin Genet. 2006 May;69(5):429-33.

11.

Mapping of DFNB12, a gene for a non-syndromal autosomal recessive deafness, to chromosome 10q21-22.

Chaib H, Place C, Salem N, Dodé C, Chardenoux S, Weissenbach J, el Zir E, Loiselet J, Petit C.

Hum Mol Genet. 1996 Jul;5(7):1061-4.

PMID:
8817348
12.

An autosomal recessive nonsyndromic-hearing-loss locus identified by DNA pooling using two inbred Bedouin kindreds.

Scott DA, Carmi R, Elbedour K, Yosefsberg S, Stone EM, Sheffield VC.

Am J Hum Genet. 1996 Aug;59(2):385-91.

13.

A gene for recessive nonsyndromic sensorineural deafness (DFNB18) maps to the chromosomal region 11p14-p15.1 containing the Usher syndrome type 1C gene.

Jain PK, Lalwani AK, Li XC, Singleton TL, Smith TN, Chen A, Deshmukh D, Verma IC, Smith RJ, Wilcox ER.

Genomics. 1998 Jun 1;50(2):290-2.

PMID:
9653658
14.

A new locus for autosomal recessive non-syndromal sensorineural hearing impairment (DFNB27) on chromosome 2q23-q31.

Pulleyn LJ, Jackson AP, Roberts E, Carridice A, Muxworthy C, Houseman M, Al-Gazali LI, Lench NJ, Markham AF, Mueller RF.

Eur J Hum Genet. 2000 Dec;8(12):991-3.

15.

DFNB48, a new nonsyndromic recessive deafness locus, maps to chromosome 15q23-q25.1.

Ahmad J, Khan SN, Khan SY, Ramzan K, Riazuddin S, Ahmed ZM, Wilcox ER, Friedman TB, Riazuddin S.

Hum Genet. 2005 Apr;116(5):407-12. Epub 2005 Feb 12.

PMID:
15711797
16.

Autosomal recessive non-syndromic deafness locus (DFNB8) maps on chromosome 21q22 in a large consanguineous kindred from Pakistan.

Veske A, Oehlmann R, Younus F, Mohyuddin A, Müller-Myhsok B, Mehdi SQ, Gal A.

Hum Mol Genet. 1996 Jan;5(1):165-8.

PMID:
8789456
17.

A human recessive neurosensory nonsyndromic hearing impairment locus is potential homologue of murine deafness (dn) locus.

Jain PK, Fukushima K, Deshmukh D, Ramesh A, Thomas E, Lalwani AK, Kumar S, Plopis B, Skarka H, Srisailapathy CR, et al.

Hum Mol Genet. 1995 Dec;4(12):2391-4.

PMID:
8634715
18.

Mutations in the lipoma HMGIC fusion partner-like 5 (LHFPL5) gene cause autosomal recessive nonsyndromic hearing loss.

Kalay E, Li Y, Uzumcu A, Uyguner O, Collin RW, Caylan R, Ulubil-Emiroglu M, Kersten FF, Hafiz G, van Wijk E, Kayserili H, Rohmann E, Wagenstaller J, Hoefsloot LH, Strom TM, Nürnberg G, Baserer N, den Hollander AI, Cremers FP, Cremers CW, Becker C, Brunner HG, Nürnberg P, Karaguzel A, Basaran S, Kubisch C, Kremer H, Wollnik B.

Hum Mutat. 2006 Jul;27(7):633-9.

PMID:
16752389
19.

USH1K, a novel locus for type I Usher syndrome, maps to chromosome 10p11.21-q21.1.

Jaworek TJ, Bhatti R, Latief N, Khan SN, Riazuddin S, Ahmed ZM.

J Hum Genet. 2012 Oct;57(10):633-7. doi: 10.1038/jhg.2012.79. Epub 2012 Jun 21.

20.

A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24.

Verhoeven K, Van Camp G, Govaerts PJ, Balemans W, Schatteman I, Verstreken M, Van Laer L, Smith RJ, Brown MR, Van de Heyning PH, Somers T, Offeciers FE, Willems PJ.

Am J Hum Genet. 1997 May;60(5):1168-73.

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