BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

139 related articles for article (PubMed ID: 10868227)

  • 1. Sensorineural hearing impairment, non-syndromic: DFNB5, 6, 7. Homozygosity mapping to localize genes causing autosomal recessive non-syndromic hearing loss.
    Fukushima K; Ueki Y; Smith RJ
    Adv Otorhinolaryngol; 2000; 56():152-7. PubMed ID: 10868227
    [No Abstract]   [Full Text] [Related]  

  • 2. DFNB15: autosomal recessive non-syndromic hearing loss gene-chromosome 3q, 19p or digenic recessive inheritance?
    Chen AH; Fukushima K; McGuirt WT; Smith RJ
    Adv Otorhinolaryngol; 2000; 56():171-5. PubMed ID: 10868231
    [No Abstract]   [Full Text] [Related]  

  • 3. Consanguineous nuclear families used to identify a new locus for recessive non-syndromic hearing loss on 14q.
    Fukushima K; Ramesh A; Srisailapathy CR; Ni L; Chen A; O'Neill M; Van Camp G; Coucke P; Smith SD; Kenyon JB
    Hum Mol Genet; 1995 Sep; 4(9):1643-8. PubMed ID: 8541854
    [TBL] [Abstract][Full Text] [Related]  

  • 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. PubMed ID: 14512973
    [TBL] [Abstract][Full Text] [Related]  

  • 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. PubMed ID: 12529709
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Pendred syndrome (goitre and sensorineural hearing loss) maps to chromosome 7 in the region containing the nonsyndromic deafness gene DFNB4.
    Coyle B; Coffey R; Armour JA; Gausden E; Hochberg Z; Grossman A; Britton K; Pembrey M; Reardon W; Trembath R
    Nat Genet; 1996 Apr; 12(4):421-3. PubMed ID: 8630497
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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. PubMed ID: 11175289
    [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. A sensorineural progressive autosomal recessive form of isolated deafness, DFNB13, maps to chromosome 7q34-q36.
    Mustapha M; Chardenoux S; Nieder A; Salem N; Weissenbach J; el-Zir E; Loiselet J; Petit C
    Eur J Hum Genet; 1998; 6(3):245-50. PubMed ID: 9781028
    [TBL] [Abstract][Full Text] [Related]  

  • 10. DFN4: non-syndromic autosomal dominant X-linked sensorineural hearing impairment.
    Pfister M; Lalwani AK
    Adv Otorhinolaryngol; 2000; 56():196-9. PubMed ID: 10868235
    [No Abstract]   [Full Text] [Related]  

  • 11. DFNB20: a novel locus for autosomal recessive, non-syndromal sensorineural hearing loss maps to chromosome 11q25-qter.
    Moynihan L; Houseman M; Newton V; Mueller R; Lench N
    Eur J Hum Genet; 1999; 7(2):243-6. PubMed ID: 10196710
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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
    Hum Mol Genet; 1995 Dec; 4(12):2391-4. PubMed ID: 8634715
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A mutation in PDS causes non-syndromic recessive deafness.
    Li XC; Everett LA; Lalwani AK; Desmukh D; Friedman TB; Green ED; Wilcox ER
    Nat Genet; 1998 Mar; 18(3):215-7. PubMed ID: 9500541
    [No Abstract]   [Full Text] [Related]  

  • 15. Deafness genes.
    Kitamura K; Takahashi K; Tamagawa Y; Noguchi Y; Kuroishikawa Y; Ishikawa K; Hagiwara H
    J Med Dent Sci; 2000 Mar; 47(1):1-11. PubMed ID: 12162522
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Genetic characteristics of recessive sensorineural hearing loss].
    Bliumina MG
    Genetika; 1987 Oct; 23(10):1897-9. PubMed ID: 3692153
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Non-syndromic progressive hearing loss DFNA38 is caused by heterozygous missense mutation in the Wolfram syndrome gene WFS1.
    Young TL; Ives E; Lynch E; Person R; Snook S; MacLaren L; Cater T; Griffin A; Fernandez B; Lee MK; King MC
    Hum Mol Genet; 2001 Oct; 10(22):2509-14. PubMed ID: 11709538
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A gene for a dominant form of non-syndromic sensorineural deafness (DFNA11) maps within the region containing the DFNB2 recessive deafness gene.
    Tamagawa Y; Kitamura K; Ishida T; Ishikawa K; Tanaka H; Tsuji S; Nishizawa M
    Hum Mol Genet; 1996 Jun; 5(6):849-52. PubMed ID: 8776602
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Identification of a new locus for autosomal dominant non-syndromic hearing impairment (DFNA7) in a large Norwegian family.
    Fagerheim T; Nilssen O; Raeymaekers P; Brox V; Moum T; Elverland HH; Teig E; Omland HH; Fostad GK; Tranebjaerg L
    Hum Mol Genet; 1996 Aug; 5(8):1187-91. PubMed ID: 8842739
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.