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 *

88 related articles for article (PubMed ID: 1463039)

  • 1. Criteria to detect minimal expressivity within families with autosomal dominant aniridia.
    Mintz-Hittner HA; Ferrell RE; Lyons LA; Kretzer FL
    Am J Ophthalmol; 1992 Dec; 114(6):700-7. PubMed ID: 1463039
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Autosomal dominant aniridia linked to the chromosome 11p13 markers catalase and D11S151 in a large Dutch family.
    Mannens M; Bleeker-Wagemakers EM; Bliek J; Hoovers J; Mandjes I; van Tol S; Frants RR; Heyting C; Westerveld A; Slater RM
    Cytogenet Cell Genet; 1989; 52(1-2):32-6. PubMed ID: 2575483
    [TBL] [Abstract][Full Text] [Related]  

  • 3. DNA diagnosis in a family with autosomal dominant aniridia.
    Verbraak FD; Mannens MA; Redeker EJ; Saunders GF; Bleeker-Wagemakers EM
    Ophthalmic Paediatr Genet; 1991 Dec; 12(4):165-70. PubMed ID: 1815167
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Resolution of the two loci for autosomal dominant aniridia, AN1 and AN2, to a single locus on chromosome 11p13.
    Lyons LA; Martha A; Mintz-Hittner HA; Saunders GF; Ferrell RE
    Genomics; 1992 Aug; 13(4):925-30. PubMed ID: 1505982
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Autosomal dominant keratitis: a possible aniridia variant.
    Pearce WG; Mielke BW; Hassard DT; Climenhaga HW; Climenhaga DB; Hodges EJ
    Can J Ophthalmol; 1995 Apr; 30(3):131-7. PubMed ID: 7627897
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Newly identified paired box 6 mutation of variant familial aniridia: Congenital iris ectropion with foveal hypoplasia.
    Kim WJ; Kim JH; Cho NC
    Indian J Ophthalmol; 2017 Jan; 65(1):55-56. PubMed ID: 28300742
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Variability of iris defects in autosomal dominant aniridia.
    Pearce WG
    Can J Ophthalmol; 1994 Feb; 29(1):25-9. PubMed ID: 8180874
    [No Abstract]   [Full Text] [Related]  

  • 8. Ocular and nonocular findings in patients with aniridia.
    Valenzuela A; Cline RA
    Can J Ophthalmol; 2004 Oct; 39(6):632-8. PubMed ID: 15559649
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Variable expressivity in autosomal dominant aniridia by clinical, electrophysiologic, and angiographic criteria.
    Hittner HM; Riccardi VM; Ferrell RE; Borda RR; Justice J
    Am J Ophthalmol; 1980 Apr; 89(4):531-9. PubMed ID: 7369316
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Aniridia].
    Liláková D; Hejcmanová D; Jüttnerová V; Rozsíval P
    Cesk Slov Oftalmol; 2002 May; 58(3):176-9. PubMed ID: 12087663
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Two anonymous DNA segments distinguish the Wilms' tumor and aniridia loci.
    Davis LM; Stallard R; Thomas GH; Couillin P; Junien C; Nowak NJ; Shows TB
    Science; 1988 Aug; 241(4867):840-2. PubMed ID: 2841760
    [TBL] [Abstract][Full Text] [Related]  

  • 12. De novo chromosome translocation t (2; 11) (p25.1; p13) in a patient with aniridia and genitourinary abnormalities.
    Hung HM; Lin SC; Su PH; Chen JY
    Acta Paediatr Taiwan; 2003; 44(2):101-3. PubMed ID: 12845852
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Detection of a cryptic paracentric inversion within band 11p13 in familial aniridia by fluorescence in situ hybridization.
    Fukushima Y; Hoovers J; Mannens M; Wakui K; Ohashi H; Ohno T; Ueoka Y; Niikawa N
    Hum Genet; 1993 Apr; 91(3):205-9. PubMed ID: 8478003
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Identification of a novel frameshift heterozygous deletion in exon 8 of the PAX6 gene in a pedigree with aniridia.
    Giray Bozkaya O; Ataman E; Aksel Kilicarslan O; Cankaya T; Ulgenalp A
    Mol Med Rep; 2016 Sep; 14(3):2150-4. PubMed ID: 27431685
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Autosomal dominant aniridia: probable linkage to acid phosphatase-1 locus on chromosome 2.
    Ferrell RE; Chakravarti A; Hittner HM; Riccardi VM
    Proc Natl Acad Sci U S A; 1980 Mar; 77(3):1580-2. PubMed ID: 6929510
    [TBL] [Abstract][Full Text] [Related]  

  • 16. An unusual cystic lesion histologically similar to autosomal dominant polycystic kidney disease in a child with aniridia and del 11p13.
    Schvimer M; Katzin WE; Shen SJ; Parulekar SG; Olsen M
    J Urol; 1994 Oct; 152(4):1218-20. PubMed ID: 8072106
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Microphthalmia, late onset keratitis, and iris coloboma/aniridia in a family with a novel PAX6 mutation.
    Xiao X; Li S; Zhang Q
    Ophthalmic Genet; 2012 Jun; 33(2):119-21. PubMed ID: 22171686
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Familial isolated aniridia associated with a translocation involving chromosomes 11 and 22 [t(11;22)(p13;q12.2)].
    Moore JW; Hyman S; Antonarakis SE; Mules EH; Thomas GH
    Hum Genet; 1986 Apr; 72(4):297-302. PubMed ID: 3754537
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Aniridia, gonadoblastoma, Wilms' tumor and deletion 11p13.
    Stefan H; Semecký V
    Acta Medica (Hradec Kralove); 1998; 41(1):29-33. PubMed ID: 9588071
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Congenital aniridia].
    Chiruţa D; Stan C
    Oftalmologia; 2014; 58(3):35-40. PubMed ID: 25842623
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.