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 *

141 related articles for article (PubMed ID: 7573044)

  • 21. 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]  

  • 22. A 5-base insertion in the gammaC-crystallin gene is associated with autosomal dominant variable zonular pulverulent cataract.
    Ren Z; Li A; Shastry BS; Padma T; Ayyagari R; Scott MH; Parks MM; Kaiser-Kupfer MI; Hejtmancik JF
    Hum Genet; 2000 May; 106(5):531-7. PubMed ID: 10914683
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. Locus heterogeneity in autosomal recessive congenital cataracts: linkage to 9q and germline HSF4 mutations.
    Forshew T; Johnson CA; Khaliq S; Pasha S; Willis C; Abbasi R; Tee L; Smith U; Trembath RC; Mehdi SQ; Moore AT; Maher ER
    Hum Genet; 2005 Sep; 117(5):452-9. PubMed ID: 15959809
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A Chinese family with progressive childhood cataracts and IVS3+1G>A CRYBA3/A1 mutations.
    Zhu Y; Shentu X; Wang W; Li J; Jin C; Yao K
    Mol Vis; 2010 Nov; 16():2347-53. PubMed ID: 21139983
    [TBL] [Abstract][Full Text] [Related]  

  • 26. CRYBA3/A1 gene mutation associated with suture-sparing autosomal dominant congenital nuclear cataract: a novel phenotype.
    Ferrini W; Schorderet DF; Othenin-Girard P; Uffer S; Héon E; Munier FL
    Invest Ophthalmol Vis Sci; 2004 May; 45(5):1436-41. PubMed ID: 15111599
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. A new locus for autosomal dominant congenital coronary cataract in a Chinese family maps to chromosome 3q.
    Liu G; Li Y; Ruan Y; Cao W; Xin L; Qian J; Gu J
    Mol Vis; 2010 May; 16():874-9. PubMed ID: 20508730
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A novel dysmorphic syndrome with open calvarial sutures and sutural cataracts maps to chromosome 14q13-q21.
    Boyadjiev SA; Justice CM; Eyaid W; McKusick VA; Lachman RS; Chowdry AB; Jabak M; Zwaan J; Wilson AF; Jabs EW
    Hum Genet; 2003 Jul; 113(1):1-9. PubMed ID: 12677423
    [TBL] [Abstract][Full Text] [Related]  

  • 30. The telomere of human chromosome 1p contains at least two independent autosomal dominant congenital cataract genes.
    McKay JD; Patterson B; Craig JE; Russell-Eggitt IM; Wirth MG; Burdon KP; Hewitt AW; Cohn AC; Kerdraon Y; Mackey DA
    Br J Ophthalmol; 2005 Jul; 89(7):831-4. PubMed ID: 15965161
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. [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]  

  • 33. 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]  

  • 34. A novel missense mutation in the gene for gap-junction protein alpha3 (GJA3) associated with autosomal dominant "nuclear punctate" cataracts linked to chromosome 13q.
    Bennett TM; Mackay DS; Knopf HL; Shiels A
    Mol Vis; 2004 Jun; 10():376-82. PubMed ID: 15208569
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. A second gene for cerulean cataracts maps to the beta crystallin region on chromosome 22.
    Kramer P; Yount J; Mitchell T; LaMorticella D; Carrero-Valenzuela R; Lovrien E; Maumenee I; Litt M
    Genomics; 1996 Aug; 35(3):539-42. PubMed ID: 8812489
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Mapping of a pedigree with autosomal dominant inherited congenital sutural cataract].
    Zhang L; Gao LH; Liu P; Li ZJ; Gao WQ; Qin W; Feng GY; Fu SB; He L
    Zhonghua Yan Ke Za Zhi; 2006 Oct; 42(10):908-12. PubMed ID: 17217785
    [TBL] [Abstract][Full Text] [Related]  

  • 38. An autosomal dominant cataract locus mapped to 19q13-qter in a Chinese family.
    Zhao R; Yang Y; He X; Liu Z; Wang P; Zhou L; Tang J; Xu W; Li L; Zhu Y
    Mol Vis; 2011 Jan; 17():265-9. PubMed ID: 21283564
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Further evidence of autosomal dominant congenital zonular pulverulent cataracts linked to 13q11 (CZP3) and a novel mutation in connexin 46 (GJA3).
    Rees MI; Watts P; Fenton I; Clarke A; Snell RG; Owen MJ; Gray J
    Hum Genet; 2000 Feb; 106(2):206-9. PubMed ID: 10746562
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A missense mutation in the human connexin50 gene (GJA8) underlies autosomal dominant "zonular pulverulent" cataract, on chromosome 1q.
    Shiels A; Mackay D; Ionides A; Berry V; Moore A; Bhattacharya S
    Am J Hum Genet; 1998 Mar; 62(3):526-32. PubMed ID: 9497259
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.