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 *

80 related articles for article (PubMed ID: 1578107)

  • 21. Ocular defects associated with a null mutation in the mouse arylamine N-acetyltransferase 2 gene.
    Wakefield L; Long H; Lack N; Sim E
    Mamm Genome; 2007 Apr; 18(4):270-6. PubMed ID: 17487534
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Histopathological characterisation of effects of the mouse Pax6(Leca4) missense mutation on eye development.
    Ramaesh T; Williams SE; Paul C; Ramaesh K; Dhillon B; West JD
    Exp Eye Res; 2009 Aug; 89(2):263-73. PubMed ID: 19345209
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Blastoderm degeneration, an early embryonic failure in dwarf Single Comb White Leghorn chickens.
    Savage TF; Mirosh LW; Jones JL; Schneiderman ET
    J Hered; 1992; 83(4):249-54. PubMed ID: 1401874
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A mutation of the WFDC1 gene is responsible for multiple ocular defects in cattle.
    Abbasi AR; Khalaj M; Tsuji T; Tanahara M; Uchida K; Sugimoto Y; Kunieda T
    Genomics; 2009 Jul; 94(1):55-62. PubMed ID: 19374945
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Duplex comb in the chicken: a multi-allelic trait.
    Somes RG
    J Hered; 1991; 82(2):169-72. PubMed ID: 2013691
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Some observations on high cavernous nostrils in the chicken.
    Somes RG
    J Hered; 1991; 82(2):172-4. PubMed ID: 2013692
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Analysis of the rdd locus in chicken: a model for human retinitis pigmentosa.
    Burt DW; Morrice DR; Lester DH; Robertson GW; Mohamed MD; Simmons I; Downey LM; Thaung C; Bridges LR; Paton IR; Gentle M; Smith J; Hocking PM; Inglehearn CF
    Mol Vis; 2003 Apr; 9():164-70. PubMed ID: 12724645
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Novel mutations in ALDH1A3 associated with autosomal recessive anophthalmia/microphthalmia, and review of the literature.
    Lin S; Harlalka GV; Hameed A; Reham HM; Yasin M; Muhammad N; Khan S; Baple EL; Crosby AH; Saleha S
    BMC Med Genet; 2018 Sep; 19(1):160. PubMed ID: 30200890
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Genetic investigation of ocular developmental genes in 52 patients with anophthalmia/microphthalmia.
    Vidya NG; Rajkumar S; Vasavada AR
    Ophthalmic Genet; 2018 Jun; 39(3):344-352. PubMed ID: 29461140
    [TBL] [Abstract][Full Text] [Related]  

  • 30. The effects of the polymorphism in exon 3 of the FAS gene on the death of chicken embryos during the incubation period.
    Wu JJ; Li WM; Zhao RX; Fang J; Wang C; Peng XL; Li X; Xiong JJ; Yang LG; Zhang SJ
    Anim Genet; 2008 Oct; 39(5):558-60. PubMed ID: 18652598
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Genetics of resistance to Salmonella typhimurium in newly hatched chicks.
    Bumstead N; Barrow PA
    Br Poult Sci; 1988 Sep; 29(3):521-9. PubMed ID: 3066449
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Autosomal Recessive Oculodentodigital Dysplasia: A Case Report and Review of the Literature.
    Taşdelen E; Durmaz CD; Karabulut HG
    Cytogenet Genome Res; 2018; 154(4):181-186. PubMed ID: 29902798
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Abnormal eye development associated with Cat4a, a dominant mouse cataract mutation on chromosome 8.
    Grimes PA; Koeberlein B; Favor J; Neuhäuser-Klaus A; Stambolian D
    Invest Ophthalmol Vis Sci; 1998 Sep; 39(10):1863-9. PubMed ID: 9727409
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Unilateral isolated microphthalmia inherited as an autosomal recessive trait.
    Fleckenstein M; Maumenee IH
    Ophthalmic Genet; 2005 Dec; 26(4):163-8. PubMed ID: 16352476
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Oculofaciocardiodental and Lenz microphthalmia syndromes result from distinct classes of mutations in BCOR.
    Ng D; Thakker N; Corcoran CM; Donnai D; Perveen R; Schneider A; Hadley DW; Tifft C; Zhang L; Wilkie AO; van der Smagt JJ; Gorlin RJ; Burgess SM; Bardwell VJ; Black GC; Biesecker LG
    Nat Genet; 2004 Apr; 36(4):411-6. PubMed ID: 15004558
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Novel mutations in BCOR in three patients with oculo-facio-cardio-dental syndrome, but none in Lenz microphthalmia syndrome.
    Horn D; Chyrek M; Kleier S; Lüttgen S; Bolz H; Hinkel GK; Korenke GC; Riess A; Schell-Apacik C; Tinschert S; Wieczorek D; Gillessen-Kaesbach G; Kutsche K
    Eur J Hum Genet; 2005 May; 13(5):563-9. PubMed ID: 15770227
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Microphthalmia With Multiple Anterior Segment Defects in Portuguese Water Dogs.
    Shaw GC; Tse MPY; Miller AD
    Vet Pathol; 2019 Mar; 56(2):269-273. PubMed ID: 30131012
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Chondrodystrophy: an inherited lethal condition in turkey embryos.
    Gaffney LJ
    J Hered; 1975; 66(6):339-43. PubMed ID: 1219057
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Microphthalmia cloudy-eye (mi(ce)): a new murine allele.
    Zimring DC; Lamoreux ML; Millichamp NJ; Skow LC
    J Hered; 1996; 87(4):334-8. PubMed ID: 8776879
    [No Abstract]   [Full Text] [Related]  

  • 40. [Genetic eye defects in the dog].
    Bouw J
    Tijdschr Diergeneeskd; 1991 Sep; 116(18):898-905. PubMed ID: 1926110
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.