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 *

96 related articles for article (PubMed ID: 9718335)

  • 1. Gene localization for aculeiform cataract, on chromosome 2q33-35.
    Héon E; Liu S; Billingsley G; Bernasconi O; Tsilfidis C; Schorderet DF; Munier FL
    Am J Hum Genet; 1998 Sep; 63(3):921-6. PubMed ID: 9718335
    [No Abstract]   [Full Text] [Related]  

  • 2. A locus for autosomal dominant anterior polar cataract on chromosome 17p.
    Berry V; Ionides AC; Moore AT; Plant C; Bhattacharya SS; Shiels A
    Hum Mol Genet; 1996 Mar; 5(3):415-9. PubMed ID: 8852669
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A novel locus of coralliform cataract mapped to chromosome 2p24-pter.
    Gao L; Qin W; Cui H; Feng G; Liu P; Gao W; Ma L; Li P; He L; Fu S
    J Hum Genet; 2005; 50(6):305-310. PubMed ID: 15933805
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Linkage of polymorphic congenital cataract to the gamma-crystallin gene locus on human chromosome 2q33-35.
    Rogaev EI; Rogaeva EA; Korovaitseva GI; Farrer LA; Petrin AN; Keryanov SA; Turaeva S; Chumakov I; St George-Hyslop P; Ginter EK
    Hum Mol Genet; 1996 May; 5(5):699-703. PubMed ID: 8733140
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A new locus for dominant "zonular pulverulent" cataract, on chromosome 13.
    Mackay D; Ionides A; Berry V; Moore A; Bhattacharya S; Shiels A
    Am J Hum Genet; 1997 Jun; 60(6):1474-8. PubMed ID: 9199569
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [An attempt to locate the gene for congenital cataracts using linkage analysis].
    Ginter EK; Petrin AN; Spitsyn VA; Rogaev EI
    Genetika; 1991 Oct; 27(10):1840-9. PubMed ID: 1778455
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A progressive early onset cataract gene maps to human chromosome 17q24.
    Armitage MM; Kivlin JD; Ferrell RE
    Nat Genet; 1995 Jan; 9(1):37-40. PubMed ID: 7704021
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Autosomal dominant congenital cataract associated with a missense mutation in the human alpha crystallin gene CRYAA.
    Litt M; Kramer P; LaMorticella DM; Murphey W; Lovrien EW; Weleber RG
    Hum Mol Genet; 1998 Mar; 7(3):471-4. PubMed ID: 9467006
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A novel locus for autosomal dominant nuclear cataract mapped to chromosome 2p12 in a Pakistani family.
    Khaliq S; Hameed A; Ismail M; Anwar K; Mehdi SQ
    Invest Ophthalmol Vis Sci; 2002 Jul; 43(7):2083-7. PubMed ID: 12091400
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A missense mutation in the gammaD crystallin gene (CRYGD) associated with autosomal dominant "coral-like" cataract linked to chromosome 2q.
    Mackay DS; Andley UP; Shiels A
    Mol Vis; 2004 Mar; 10():155-62. PubMed ID: 15041957
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A new locus for autosomal dominant cataract on chromosome 19: linkage analyses and screening of candidate genes.
    Bateman JB; Richter L; Flodman P; Burch D; Brown S; Penrose P; Paul O; Geyer DD; Brooks DG; Spence MA
    Invest Ophthalmol Vis Sci; 2006 Aug; 47(8):3441-9. PubMed ID: 16877414
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A novel form of "central pouchlike" cataract, with sutural opacities, maps to chromosome 15q21-22.
    Vanita ; Singh JR; Sarhadi VK; Singh D; Reis A; Rueschendorf F; Becker-Follmann J; Jung M; Sperling K
    Am J Hum Genet; 2001 Feb; 68(2):509-14. PubMed ID: 11133359
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Autosomal dominant retinitis pigmentosa (ADRP): localization of an ADRP gene to the long arm of chromosome 3.
    McWilliam P; Farrar GJ; Kenna P; Bradley DG; Humphries MM; Sharp EM; McConnell DJ; Lawler M; Sheils D; Ryan C
    Genomics; 1989 Oct; 5(3):619-22. PubMed ID: 2613244
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A locus for autosomal dominant posterior polar cataract on chromosome 1p.
    Ionides AC; Berry V; Mackay DS; Moore AT; Bhattacharya SS; Shiels A
    Hum Mol Genet; 1997 Jan; 6(1):47-51. PubMed ID: 9002669
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Linkage of a locus for autosomal dominant familial spastic paraplegia to chromosome 2p markers.
    Hentati A; Pericak-Vance MA; Lennon F; Wasserman B; Hentati F; Juneja T; Angrist MH; Hung WY; Boustany RM; Bohlega S
    Hum Mol Genet; 1994 Oct; 3(10):1867-71. PubMed ID: 7849714
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Assignment of congenital cataract Volkmann type (CCV) to chromosome 1p36.
    Eiberg H; Lund AM; Warburg M; Rosenberg T
    Hum Genet; 1995 Jul; 96(1):33-8. PubMed ID: 7607651
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Autosomal dominant congenital cataract. Morphology and genetic mapping.
    Marner E; Rosenberg T; Eiberg H
    Acta Ophthalmol (Copenh); 1989 Apr; 67(2):151-8. PubMed ID: 2728866
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Linkage of hereditary distal myopathy with desmin accumulation to 2q.
    Saavedra-Matiz CA; Chapman NH; Wijsman EM; Horowitz SH; Rosen DR
    Hum Hered; 2000; 50(3):166-70. PubMed ID: 10686494
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A new locus for autosomal dominant posterior polar cataract in Moroccan Jews maps to chromosome 14q22-23.
    Pras E; Mahler O; Kumar V; Frydman M; Gefen N; Pras E; Hejtmancik JF
    J Med Genet; 2006 Oct; 43(10):e50. PubMed ID: 17047090
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Fine mapping of PPH1, a gene for familial primary pulmonary hypertension, to a 3-cM region on chromosome 2q33.
    Deng Z; Haghighi F; Helleby L; Vanterpool K; Horn EM; Barst RJ; Hodge SE; Morse JH; Knowles JA
    Am J Respir Crit Care Med; 2000 Mar; 161(3 Pt 1):1055-9. PubMed ID: 10712363
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.