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 *

221 related articles for article (PubMed ID: 7634534)

  • 1. Autosomal recessive retinitis pigmentosa locus maps on chromosome 1q in a large consanguineous family from Pakistan.
    Leutelt J; Oehlmann R; Younus F; van den Born LI; Weber JL; Denton MJ; Mehdi SQ; Gal A
    Clin Genet; 1995 Mar; 47(3):122-4. PubMed ID: 7634534
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Fine mapping of the autosomal recessive retinitis pigmentosa locus (RP12) on chromosome 1q; exclusion of the phosducin gene (PDC).
    van Soest S; te Nijenhuis S; van den Born LI; Bleeker-Wagemakers EM; Sharp E; Sandkuijl LA; Westerveld A; Bergen AA
    Cytogenet Cell Genet; 1996; 73(1-2):81-5. PubMed ID: 8646891
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. A novel locus for autosomal recessive retinitis pigmentosa in a consanguineous Pakistani family maps to chromosome 2p.
    Naz S; Riazuddin SA; Li L; Shahid M; Kousar S; Sieving PA; Hejtmancik JF; Riazuddin S
    Am J Ophthalmol; 2010 May; 149(5):861-6. PubMed ID: 20227676
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Assignment of a gene for autosomal recessive retinitis pigmentosa (RP12) to chromosome 1q31-q32.1 in an inbred and genetically heterogeneous disease population.
    van Soest S; van den Born LI; Gal A; Farrar GJ; Bleeker-Wagemakers LM; Westerveld A; Humphries P; Sandkuijl LA; Bergen AA
    Genomics; 1994 Aug; 22(3):499-504. PubMed ID: 8001962
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Association of pathogenic mutations in TULP1 with retinitis pigmentosa in consanguineous Pakistani families.
    Iqbal M; Naeem MA; Riazuddin SA; Ali S; Farooq T; Qazi ZA; Khan SN; Husnain T; Riazuddin S; Sieving PA; Hejtmancik JF; Riazuddin S
    Arch Ophthalmol; 2011 Oct; 129(10):1351-7. PubMed ID: 21987678
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A ninth locus (RP18) for autosomal dominant retinitis pigmentosa maps in the pericentromeric region of chromosome 1.
    Xu SY; Schwartz M; Rosenberg T; Gal A
    Hum Mol Genet; 1996 Aug; 5(8):1193-7. PubMed ID: 8842740
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A new autosomal recessive retinitis pigmentosa locus maps on chromosome 2q31-q33.
    Bayés M; Goldaracena B; Martínez-Mir A; Iragui-Madoz MI; Solans T; Chivelet P; Bussaglia E; Ramos-Arroyo MA; Baiget M; Vilageliu L; Balcells S; Gonzàlez-Duarte R; Grinberg D
    J Med Genet; 1998 Feb; 35(2):141-5. PubMed ID: 9507394
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Autosomal recessive retinitis pigmentosa is associated with mutations in RP1 in three consanguineous Pakistani families.
    Riazuddin SA; Zulfiqar F; Zhang Q; Sergeev YV; Qazi ZA; Husnain T; Caruso R; Riazuddin S; Sieving PA; Hejtmancik JF
    Invest Ophthalmol Vis Sci; 2005 Jul; 46(7):2264-70. PubMed ID: 15980210
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Autosomal recessive retinitis pigmentosa locus RP28 maps between D2S1337 and D2S286 on chromosome 2p11-p15 in an Indian family.
    Gu S; Kumaramanickavel G; Srikumari CR; Denton MJ; Gal A
    J Med Genet; 1999 Sep; 36(9):705-7. PubMed ID: 10507729
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A new locus for autosomal recessive retinitis pigmentosa (RP19) maps to 1p13-1p21.
    Martínez-Mir A; Bayés M; Vilageliu L; Grinberg D; Ayuso C; del Río T; García-Sandoval B; Bussaglia E; Baiget M; Gonzàlez-Duarte R; Balcells S
    Genomics; 1997 Feb; 40(1):142-6. PubMed ID: 9070931
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Refinement of the locus for autosomal recessive Retinitis pigmentosa (RP25) linked to chromosome 6q in a family of Pakistani origin.
    Khaliq S; Hameed A; Ismail M; Mehdi SQ; Bessant DA; Payne AM; Bhattacharya SS
    Am J Hum Genet; 1999 Aug; 65(2):571-4. PubMed ID: 10417302
    [No Abstract]   [Full Text] [Related]  

  • 14. 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]  

  • 15. Splice-site mutations identified in PDE6A responsible for retinitis pigmentosa in consanguineous Pakistani families.
    Khan SY; Ali S; Naeem MA; Khan SN; Husnain T; Butt NH; Qazi ZA; Akram J; Riazuddin S; Ayyagari R; Hejtmancik JF; Riazuddin SA
    Mol Vis; 2015; 21():871-82. PubMed ID: 26321862
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. Confirmation of linkage and refinement of the RP28 locus for autosomal recessive retinitis pigmentosa on chromosome 2p14-p15 in an Indian family.
    Kumar A; Shetty J; Kumar B; Blanton SH
    Mol Vis; 2004 Jun; 10():399-402. PubMed ID: 15215745
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Evidence for a novel autosomal dominant retinitis pigmentosa linked to chromosome 1p22.1-q12 in a Chinese family.
    Yuan Y; Zhou X; Wang F; Yan M; Ding F
    Curr Eye Res; 2011 Feb; 36(2):154-67. PubMed ID: 21281067
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Homozygosity mapping of autosomal recessive retinitis pigmentosa locus (RP22) on chromosome 16p12.1-p12.3.
    Finckh U; Xu S; Kumaramanickavel G; Schürmann M; Mukkadan JK; Fernandez ST; John S; Weber JL; Denton MJ; Gal A
    Genomics; 1998 Mar; 48(3):341-5. PubMed ID: 9545639
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.