BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

199 related articles for article (PubMed ID: 17211611)

  • 1. 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. PubMed ID: 17211611
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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. PubMed ID: 17166180
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Localization of a novel autosomal recessive non-syndromic hearing impairment locus DFNB55 to chromosome 4q12-q13.2.
    Irshad S; Santos RL; Muhammad D; Lee K; McArthur N; Haque S; Ahmad W; Leal SM
    Clin Genet; 2005 Sep; 68(3):262-7. PubMed ID: 16098016
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A new autosomal recessive nonsyndromic hearing impairment locus DFNB96 on chromosome 1p36.31-p36.13.
    Ansar M; Lee K; Naqvi SK; Andrade PB; Basit S; Santos-Cortez RL; Ahmad W; Leal SM
    J Hum Genet; 2011 Dec; 56(12):866-8. PubMed ID: 21937999
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Localization of a novel autosomal recessive nonsyndromic hearing impairment locus DFNB65 to chromosome 20q13.2-q13.32.
    Tariq A; Santos RL; Khan MN; Lee K; Hassan MJ; Ahmad W; Leal SM
    J Mol Med (Berl); 2006 Jun; 84(6):484-90. PubMed ID: 16596430
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genome-wide analysis reveals a novel autosomal-recessive hearing loss locus DFNB80 on chromosome 2p16.1-p21.
    Ali Mosrati M; Schrauwen I; Ben Saiid M; Aifa-Hmani M; Fransen E; Mneja M; Ghorbel A; Van Camp G; Masmoudi S
    J Hum Genet; 2013 Feb; 58(2):98-101. PubMed ID: 23235334
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Novel autosomal recessive nonsyndromic hearing impairment locus DFNB90 maps to 7p22.1-p15.3.
    Ali G; Lee K; Andrade PB; Basit S; Santos-Cortez RL; Chen L; Jelani M; Ansar M; Ahmad W; Leal SM
    Hum Hered; 2011; 71(2):106-12. PubMed ID: 21734401
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mapping of a new autosomal recessive nonsyndromic hearing loss locus (DFNB32) to chromosome 1p13.3-22.1.
    Masmoudi S; Tlili A; Majava M; Ghorbel AM; Chardenoux S; Lemainque A; Zina ZB; Moala J; Männikkö M; Weil D; Lathrop M; Ala-Kokko L; Drira M; Petit C; Ayadi H
    Eur J Hum Genet; 2003 Feb; 11(2):185-8. PubMed ID: 12634867
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. A novel locus for autosomal dominant nonsyndromic hearing loss (DFNA44) maps to chromosome 3q28-29.
    Modamio-Høybjør S; Moreno-Pelayo MA; Mencía A; del Castillo I; Chardenoux S; Armenta D; Lathrop M; Petit C; Moreno F
    Hum Genet; 2003 Jan; 112(1):24-8. PubMed ID: 12483295
    [TBL] [Abstract][Full Text] [Related]  

  • 12. DFNB74, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 12q14.2-q15.
    Waryah AM; Rehman A; Ahmed ZM; Bashir ZH; Khan SY; Zafar AU; Riazuddin S; Friedman TB; Riazuddin S
    Clin Genet; 2009 Sep; 76(3):270-5. PubMed ID: 19650862
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A novel autosomal recessive nonsyndromic hearing impairment locus (DFNB42) maps to chromosome 3q13.31-q22.3.
    Aslam M; Wajid M; Chahrour MH; Ansar M; Haque S; Pham TL; Santos RP; Yan K; Ahmad W; Leal SM
    Am J Med Genet A; 2005 Feb; 133A(1):18-22. PubMed ID: 15641023
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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. PubMed ID: 16650082
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Novel autosomal recessive non-syndromic hearing impairment locus (DFNB71) maps to chromosome 8p22-21.3.
    Chishti MS; Lee K; McDonald ML; Hassan MJ; Ansar M; Ahmad W; Leal SM
    J Hum Genet; 2009 Mar; 54(3):141-4. PubMed ID: 19229252
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Splice-site mutations in the TRIC gene underlie autosomal recessive nonsyndromic hearing impairment in Pakistani families.
    Chishti MS; Bhatti A; Tamim S; Lee K; McDonald ML; Leal SM; Ahmad W
    J Hum Genet; 2008; 53(2):101-105. PubMed ID: 18084694
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A novel autosomal recessive non-syndromic hearing impairment locus (DFNB47) maps to chromosome 2p25.1-p24.3.
    Hassan MJ; Santos RL; Rafiq MA; Chahrour MH; Pham TL; Wajid M; Hijab N; Wambangco M; Lee K; Ansar M; Yan K; Ahmad W; Leal SM
    Hum Genet; 2006 Jan; 118(5):605-10. PubMed ID: 16261342
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Digenic inheritance of an autosomal recessive hypotrichosis in two consanguineous pedigrees.
    Basit S; Wali A; Aziz A; Muhammad N; Jelani M; Ahmad W
    Clin Genet; 2011 Mar; 79(3):273-81. PubMed ID: 20528890
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mapping of a novel autosomal recessive nonsyndromic deafness locus (DFNB46) to chromosome 18p11.32-p11.31.
    Mir A; Ansar M; Chahrour MH; Pham TL; Wajid M; Haque S; Yan K; Ahmad W; Leal SM
    Am J Med Genet A; 2005 Feb; 133A(1):23-6. PubMed ID: 15637723
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.