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 *

111 related articles for article (PubMed ID: 9402956)

  • 1. Fine mapping of the gene for autosomal dominant juvenile-onset glaucoma with iridogoniodysgenesis in 6p25-tel.
    Graff C; Jerndal T; Wadelius C
    Hum Genet; 1997 Dec; 101(2):130-4. PubMed ID: 9402956
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Familial glaucoma iridogoniodysplasia maps to a 6p25 region implicated in primary congenital glaucoma and iridogoniodysgenesis anomaly.
    Jordan T; Ebenezer N; Manners R; McGill J; Bhattacharya S
    Am J Hum Genet; 1997 Oct; 61(4):882-8. PubMed ID: 9382099
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Autosomal dominant iridogoniodysgenesis anomaly maps to 6p25.
    Mears AJ; Mirzayans F; Gould DB; Pearce WG; Walter MA
    Am J Hum Genet; 1996 Dec; 59(6):1321-7. PubMed ID: 8940278
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Autosomal-dominant iridogoniodysgenesis and Axenfeld-Rieger syndrome are genetically distinct.
    Walter MA; Mirzayans F; Mears AJ; Hickey K; Pearce WG
    Ophthalmology; 1996 Nov; 103(11):1907-15. PubMed ID: 8942889
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A gene for primary congenital glaucoma is not linked to the locus on chromosome 1q for autosomal dominant juvenile-onset open angle glaucoma.
    Anderson KL; Lewis RA; Bejjani BA; Baird L; Otterud B; Tomey KF; Astle WF; Dueker DK; Leppert M; Lupski JR
    J Glaucoma; 1996 Dec; 5(6):416-21. PubMed ID: 8946299
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Ocular developmental abnormalities and glaucoma associated with interstitial 6p25 duplications and deletions.
    Lehmann OJ; Ebenezer ND; Ekong R; Ocaka L; Mungall AJ; Fraser S; McGill JI; Hitchings RA; Khaw PT; Sowden JC; Povey S; Walter MA; Bhattacharya SS; Jordan T
    Invest Ophthalmol Vis Sci; 2002 Jun; 43(6):1843-9. PubMed ID: 12036988
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Linkage of autosomal dominant iris hypoplasia to the region of the Rieger syndrome locus (4q25).
    Héon E; Sheth BP; Kalenak JW; Sunden SL; Streb LM; Taylor CM; Alward WL; Sheffield VC; Stone EM
    Hum Mol Genet; 1995 Aug; 4(8):1435-9. PubMed ID: 7581385
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Localization of a locus (GLC1B) for adult-onset primary open angle glaucoma to the 2cen-q13 region.
    Stoilova D; Child A; Trifan OC; Crick RP; Coakes RL; Sarfarazi M
    Genomics; 1996 Aug; 36(1):142-50. PubMed ID: 8812425
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Clinical features of five pedigrees genetically linked to the juvenile glaucoma locus on chromosome 1q21-q31.
    Wiggs JL; Del Bono EA; Schuman JS; Hutchinson BT; Walton DS
    Ophthalmology; 1995 Dec; 102(12):1782-9. PubMed ID: 9098278
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetic linkage of autosomal dominant juvenile glaucoma to 1q21-q31 in three affected pedigrees.
    Wiggs JL; Haines JL; Paglinauan C; Fine A; Sporn C; Lou D
    Genomics; 1994 May; 21(2):299-303. PubMed ID: 8088822
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Autosomal dominant iridogoniodysgenesis: glaucoma management.
    Wyatt HT; Pearce WG; Boyd TA; Ombres RS; Salter AB
    Can J Ophthalmol; 1983 Feb; 18(1):11-4. PubMed ID: 6839197
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Autosomal dominant iridogoniodysgenesis: genetic features.
    Pearce WG; Wyatt HT; Boyd TA; Ombres RS; Salter AB
    Can J Ophthalmol; 1983 Feb; 18(1):7-10. PubMed ID: 6839205
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Confirmation of linkage to 1q21-31 in a Danish autosomal dominant juvenile-onset glaucoma family and evidence of genetic heterogeneity.
    Graff C; Urbak SF; Jerndal T; Wadelius C
    Hum Genet; 1995 Sep; 96(3):285-9. PubMed ID: 7649543
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A second locus (GLC3B) for primary congenital glaucoma (Buphthalmos) maps to the 1p36 region.
    Akarsu AN; Turacli ME; Aktan SG; Barsoum-Homsy M; Chevrette L; Sayli BS; Sarfarazi M
    Hum Mol Genet; 1996 Aug; 5(8):1199-203. PubMed ID: 8842741
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Adult-onset primary open angle glaucoma does not localize to chromosome 2cen-q13 in North American families.
    Allingham RR; Wiggs JL; Damji KF; Herndon L; Youn J; Tallett DA; Jones KH; Del Bono EA; Reardon M; Haines JL; Pericak-Vance MA
    Hum Hered; 1998; 48(5):251-5. PubMed ID: 9748694
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Axenfeld-Rieger syndrome in the age of molecular genetics.
    Alward WL
    Am J Ophthalmol; 2000 Jul; 130(1):107-15. PubMed ID: 11004268
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mapping of a gene for autosomal dominant juvenile-onset open-angle glaucoma to chromosome Iq.
    Richards JE; Lichter PR; Boehnke M; Uro JL; Torrez D; Wong D; Johnson AT
    Am J Hum Genet; 1994 Jan; 54(1):62-70. PubMed ID: 8279471
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Glaucoma genetics: where are we? Where will we go?
    Craig JE; Mackey DA
    Curr Opin Ophthalmol; 1999 Apr; 10(2):126-34. PubMed ID: 10537763
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genetic linkage of autosomal dominant primary open angle glaucoma to chromosome 3q in a Greek pedigree.
    Kitsos G; Eiberg H; Economou-Petersen E; Wirtz MK; Kramer PL; Aspiotis M; Tommerup N; Petersen MB; Psilas K
    Eur J Hum Genet; 2001 Jun; 9(6):452-7. PubMed ID: 11436127
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Evidence that a locus for familial high myopia maps to chromosome 18p.
    Young TL; Ronan SM; Drahozal LA; Wildenberg SC; Alvear AB; Oetting WS; Atwood LD; Wilkin DJ; King RA
    Am J Hum Genet; 1998 Jul; 63(1):109-19. PubMed ID: 9634508
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.