These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

183 related articles for article (PubMed ID: 8755925)

  • 1. 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. PubMed ID: 8755925
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Familial hypomagnesemia maps to chromosome 9q, not to the X chromosome: genetic linkage mapping and analysis of a balanced translocation breakpoint.
    Walder RY; Shalev H; Brennan TM; Carmi R; Elbedour K; Scott DA; Hanauer A; Mark AL; Patil S; Stone EM; Sheffield VC
    Hum Mol Genet; 1997 Sep; 6(9):1491-7. PubMed ID: 9285786
    [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. Localization of the gene for thiamine-responsive megaloblastic anemia syndrome, on the long arm of chromosome 1, by homozygosity mapping.
    Neufeld EJ; Mandel H; Raz T; Szargel R; Yandava CN; Stagg A; Fauré S; Barrett T; Buist N; Cohen N
    Am J Hum Genet; 1997 Dec; 61(6):1335-41. PubMed ID: 9399900
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. An autosomal recessive nonsyndromic form of sensorineural hearing loss maps to 3p-DFNB6.
    Fukushima K; Ramesh A; Srisailapathy CR; Ni L; Wayne S; O'Neill ME; Van Camp G; Coucke P; Jain P; Wilcox ER; Smith SD; Kenyon JB; Zbar RI; Smith RJ
    Genome Res; 1995 Oct; 5(3):305-8. PubMed ID: 8593615
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 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. Candidate locus for a nuclear modifier gene for maternally inherited deafness.
    Bykhovskaya Y; Estivill X; Taylor K; Hang T; Hamon M; Casano RA; Yang H; Rotter JI; Shohat M; Fischel-Ghodsian N
    Am J Hum Genet; 2000 Jun; 66(6):1905-10. PubMed ID: 10788333
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Construction of P1-derived artificial chromosome and yeast artificial chromosome contigs encompassing the DFNB7 and DFNB11 region of chromosome 9q13-21.
    Greinwald JH; Scott DA; Marietta JR; Carmi R; Manaligod J; Ramesh A; Zbar RI; Kraft ML; Elbedour K; Yairi Y; Musy M; Skvorak AB; Van Camp G; Srisailapathy CR; Lovett M; Morton CC; Sheffield VC; Smith RJ
    Genome Res; 1997 Sep; 7(9):879-86. PubMed ID: 9314493
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Nonsyndromic autosomal recessive deafness is linked to the DFNB1 locus in a large inbred Bedouin family from Israel.
    Scott DA; Carmi R; Elbedour K; Duyk GM; Stone EM; Sheffield VC
    Am J Hum Genet; 1995 Oct; 57(4):965-8. PubMed ID: 7573061
    [No Abstract]   [Full Text] [Related]  

  • 12. 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]  

  • 13. A Bedouin kindred with infantile nephronophthisis demonstrates linkage to chromosome 9 by homozygosity mapping.
    Haider NB; Carmi R; Shalev H; Sheffield VC; Landau D
    Am J Hum Genet; 1998 Nov; 63(5):1404-10. PubMed ID: 9792867
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Evidence for linkage between Wilson disease and esterase D in three kindreds: detection of linkage for an autosomal recessive disorder by the family study method.
    Bonné-Tamir B; Farrer LA; Frydman M; Kanaaneh H
    Genet Epidemiol; 1986; 3(3):201-9. PubMed ID: 3459695
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. 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]  

  • 18. Autosomal recessive catecholamine- or exercise-induced polymorphic ventricular tachycardia: clinical features and assignment of the disease gene to chromosome 1p13-21.
    Lahat H; Eldar M; Levy-Nissenbaum E; Bahan T; Friedman E; Khoury A; Lorber A; Kastner DL; Goldman B; Pras E
    Circulation; 2001 Jun; 103(23):2822-7. PubMed ID: 11401939
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Localization of a novel gene for nonsyndromic hearing loss (DFNB17) to chromosome region 7q31.
    Greinwald JH; Wayne S; Chen AH; Scott DA; Zbar RI; Kraft ML; Prasad S; Ramesh A; Coucke P; Srisailapathy CR; Lovett M; Van Camp G; Smith RJ
    Am J Med Genet; 1998 Jun; 78(2):107-13. PubMed ID: 9674898
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic mapping of the gene for Usher syndrome: linkage analysis in a large Samaritan kindred.
    Bonné-Tamir B; Korostishevsky M; Kalinsky H; Seroussi E; Beker R; Weiss S; Godel V
    Genomics; 1994 Mar; 20(1):36-42. PubMed ID: 8020954
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.