114 related articles for article (PubMed ID: 26305302)
1. Molecular Distribution of Deafness Loci in Various Ethnic Groups of the Punjab, Pakistan.
Ullah S; Aslamkhan M; Rasheed A
J Coll Physicians Surg Pak; 2015 Aug; 25(8):573-8. PubMed ID: 26305302
[TBL] [Abstract][Full Text] [Related]
2. 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. PubMed ID: 8789456
[TBL] [Abstract][Full Text] [Related]
3. 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. PubMed ID: 12529709
[TBL] [Abstract][Full Text] [Related]
4. Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23.
Bork JM; Peters LM; Riazuddin S; Bernstein SL; Ahmed ZM; Ness SL; Polomeno R; Ramesh A; Schloss M; Srisailpathy CR; Wayne S; Bellman S; Desmukh D; Ahmed Z; Khan SN; Kaloustian VM; Li XC; Lalwani A; Riazuddin S; Bitner-Glindzicz M; Nance WE; Liu XZ; Wistow G; Smith RJ; Griffith AJ; Wilcox ER; Friedman TB; Morell RJ
Am J Hum Genet; 2001 Jan; 68(1):26-37. PubMed ID: 11090341
[TBL] [Abstract][Full Text] [Related]
5. Localization of a novel autosomal recessive non-syndromic hearing impairment locus (DFNB38) to 6q26-q27 in a consanguineous kindred from Pakistan.
Ansar M; Ramzan M; Pham TL; Yan K; Jamal SM; Haque S; Ahmad W; Leal SM
Hum Hered; 2003; 55(1):71-4. PubMed ID: 12890929
[TBL] [Abstract][Full Text] [Related]
6. 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. PubMed ID: 17066295
[TBL] [Abstract][Full Text] [Related]
7. [Preliminary linkage analysis of a Chinese family with benign familial infantile convulsion].
Xiong G; Deng FY; Xiao B; Yang XS; Ning JC; Wu ZG; Wang K; Deng HW
Zhonghua Er Ke Za Zhi; 2004 Jun; 42(6):424-8. PubMed ID: 15265426
[TBL] [Abstract][Full Text] [Related]
8. 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. PubMed ID: 11973626
[TBL] [Abstract][Full Text] [Related]
9. Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafness.
Masmoudi S; Antonarakis SE; Schwede T; Ghorbel AM; Gratri M; Pappasavas MP; Drira M; Elgaied-Boulila A; Wattenhofer M; Rossier C; Scott HS; Ayadi H; Guipponi M
Hum Mutat; 2001 Aug; 18(2):101-8. PubMed ID: 11462234
[TBL] [Abstract][Full Text] [Related]
10. 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. PubMed ID: 8817348
[TBL] [Abstract][Full Text] [Related]
11. Linkage analysis of hearing impairment in families of Bannu Distric.
; Khan J; Ismail M; Rafi M; ; Jalal A
J Pak Med Assoc; 2019 Nov; 69(11):1632-1636. PubMed ID: 31740869
[TBL] [Abstract][Full Text] [Related]
12. Contribution of DFNB1 and DFNB2 loci to neurosensory deafness in affected Tunisian families.
Boulila-Elgaïed A; Masmoudi S; Drira M; Gouia M; Chaib H; Petit C; Ayadi H
Arch Inst Pasteur Tunis; 1997; 74(1-2):5-8. PubMed ID: 15945170
[TBL] [Abstract][Full Text] [Related]
13. DFNB68, a novel autosomal recessive non-syndromic hearing impairment locus at chromosomal region 19p13.2.
Santos RL; Hassan MJ; Sikandar S; Lee K; Ali G; Martin PE; Wambangco MA; Ahmad W; Leal SM
Hum Genet; 2006 Aug; 120(1):85-92. PubMed ID: 16703383
[TBL] [Abstract][Full Text] [Related]
14. Autosomal recessive retinitis pigmentosa in a Pakistani family mapped to CNGA1 with identification of a novel mutation.
Zhang Q; Zulfiqar F; Riazuddin SA; Xiao X; Ahmad Z; Riazuddin S; Hejtmancik JF
Mol Vis; 2004 Nov; 10():884-9. PubMed ID: 15570217
[TBL] [Abstract][Full Text] [Related]
15. Linkage studies of non-syndromic recessive deafness (NSRD) in a family originating from the Mirpur region of Pakistan maps DFNB1 centromeric to D13S175.
Brown KA; Janjua AH; Karbani G; Parry G; Noble A; Crockford G; Bishop DT; Newton VE; Markham AF; Mueller RF
Hum Mol Genet; 1996 Jan; 5(1):169-73. PubMed ID: 8789457
[TBL] [Abstract][Full Text] [Related]
16. A non-syndrome form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q.
Guilford P; Ben Arab S; Blanchard S; Levilliers J; Weissenbach J; Belkahia A; Petit C
Nat Genet; 1994 Jan; 6(1):24-8. PubMed ID: 8136828
[TBL] [Abstract][Full Text] [Related]
17. Linkage of autosomal dominant hearing loss to the short arm of chromosome 1 in two families.
Coucke P; Van Camp G; Djoyodiharjo B; Smith SD; Frants RR; Padberg GW; Darby JK; Huizing EH; Cremers CW; Kimberling WJ
N Engl J Med; 1994 Aug; 331(7):425-31. PubMed ID: 8035838
[TBL] [Abstract][Full Text] [Related]
18. Mapping of three novel loci for non-syndromic autosomal recessive mental retardation (NS-ARMR) in consanguineous families from Pakistan.
Rafiq MA; Ansar M; Marshall CR; Noor A; Shaheen N; Mowjoodi A; Khan MA; Ali G; Amin-ud-Din M; Feuk L; Vincent JB; Scherer SW
Clin Genet; 2010 Nov; 78(5):478-83. PubMed ID: 20345473
[TBL] [Abstract][Full Text] [Related]
19. A new locus for autosomal recessive RP (RP29) mapping to chromosome 4q32-q34 in a Pakistani family.
Hameed A; Khaliq S; Ismail M; Anwar K; Mehdi SQ; Bessant D; Payne AM; Bhattacharya SS
Invest Ophthalmol Vis Sci; 2001 Jun; 42(7):1436-8. PubMed ID: 11381043
[TBL] [Abstract][Full Text] [Related]
20. Mutations of MYO6 are associated with recessive deafness, DFNB37.
Ahmed ZM; Morell RJ; Riazuddin S; Gropman A; Shaukat S; Ahmad MM; Mohiddin SA; Fananapazir L; Caruso RC; Husnain T; Khan SN; Riazuddin S; Griffith AJ; Friedman TB; Wilcox ER
Am J Hum Genet; 2003 May; 72(5):1315-22. PubMed ID: 12687499
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
