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 *

102 related articles for article (PubMed ID: 8723718)

  • 21. A novel keratocan mutation causing autosomal recessive cornea plana.
    Lehmann OJ; El-ashry MF; Ebenezer ND; Ocaka L; Francis PJ; Wilkie SE; Patel RJ; Ficker L; Jordan T; Khaw PT; Bhattacharya SS
    Invest Ophthalmol Vis Sci; 2001 Dec; 42(13):3118-22. PubMed ID: 11726611
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Linkage of posterior polymorphous corneal dystrophy to 20q11.
    Héon E; Mathers WD; Alward WL; Weisenthal RW; Sunden SL; Fishbaugh JA; Taylor CM; Krachmer JH; Sheffield VC; Stone EM
    Hum Mol Genet; 1995 Mar; 4(3):485-8. PubMed ID: 7795607
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Genetic heterogeneity of dominantly inherited olivopontocerebellar atrophy (OPCA) in the Japanese: linkage study of two pedigrees and evidence for the disease locus on chromosome 12q (SCA2).
    Ihara T; Sasaki H; Wakisaka A; Takada A; Yoshiki T; Matsuura T; Hamada T; Suzuki Y; Tashiro K
    Jpn J Hum Genet; 1994 Sep; 39(3):305-13. PubMed ID: 7841441
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Congenital stromal dystrophy of the cornea caused by a mutation in the decorin gene.
    Bredrup C; Knappskog PM; Majewski J; Rødahl E; Boman H
    Invest Ophthalmol Vis Sci; 2005 Feb; 46(2):420-6. PubMed ID: 15671264
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Assignment of granular corneal dystrophy Groenouw type I (CDGG1) to chromosome 5q.
    Eiberg H; Møller HU; Berendt I; Mohr J
    Eur J Hum Genet; 1994; 2(2):132-8. PubMed ID: 8044658
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A locus for posterior polymorphous corneal dystrophy (PPCD3) maps to chromosome 10.
    Shimizu S; Krafchak C; Fuse N; Epstein MP; Schteingart MT; Sugar A; Eibschitz-Tsimhoni M; Downs CA; Rozsa F; Trager EH; Reed DM; Boehnke M; Moroi SE; Richards JE
    Am J Med Genet A; 2004 Nov; 130A(4):372-7. PubMed ID: 15384081
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Evidence for further genetic locus heterogeneity and confirmation of RLS-1 in restless legs syndrome.
    Winkelmann J; Lichtner P; Pütz B; Trenkwalder C; Hauk S; Meitinger T; Strom T; Muller-Myhsok B
    Mov Disord; 2006 Jan; 21(1):28-33. PubMed ID: 16124010
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Fine mapping of the Schnyder's crystalline corneal dystrophy locus.
    Theendakara V; Tromp G; Kuivaniemi H; White PS; Panchal S; Cox J; Winters RS; Riebeling P; Tost F; Hoeltzenbein M; Tervo TM; Henn W; Denniger E; Krause M; Koksal M; Kargi S; Ugurbas SH; Latvala T; Shearman AM; Weiss JS
    Hum Genet; 2004 May; 114(6):594-600. PubMed ID: 15034782
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Homozygosity mapping and linkage analysis demonstrate that autosomal recessive congenital hereditary endothelial dystrophy (CHED) and autosomal dominant CHED are genetically distinct.
    Callaghan M; Hand CK; Kennedy SM; FitzSimon JS; Collum LM; Parfrey NA
    Br J Ophthalmol; 1999 Jan; 83(1):115-9. PubMed ID: 10209448
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Autosomal recessive corneal endothelial dystrophy (CHED2) is associated with mutations in SLC4A11.
    Jiao X; Sultana A; Garg P; Ramamurthy B; Vemuganti GK; Gangopadhyay N; Hejtmancik JF; Kannabiran C
    J Med Genet; 2007 Jan; 44(1):64-8. PubMed ID: 16825429
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Familial subepithelial corneal amyloidosis (gelatinous drop-like corneal dystrophy): exclusion of linkage to lactoferrin gene.
    Klintworth GK; Sommer JR; Obrian G; Han L; Ahmed MN; Qumsiyeh MB; Lin PY; Basti S; Reddy MK; Kanai A; Hotta Y; Sugar J; Kumaramanickavel G; Munier F; Schorderet DF; El Matri L; Iwata F; Kaiser-Kupfer M; Nagata M; Nakayasu K; Hejtmancik JF; Teng CT
    Mol Vis; 1998 Dec; 4():31. PubMed ID: 9873069
    [TBL] [Abstract][Full Text] [Related]  

  • 32. North Carolina macular dystrophy (MCDR1) caused by a novel tandem duplication of the
    Bowne SJ; Sullivan LS; Wheaton DK; Locke KG; Jones KD; Koboldt DC; Fulton RS; Wilson RK; Blanton SH; Birch DG; Daiger SP
    Mol Vis; 2016; 22():1239-1247. PubMed ID: 27777503
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Fine mapping of the Darier's disease locus on chromosome 12q.
    Richard G; Wright AR; Harris S; Doyle SZ; Korge B; Mazzanti C; Tanaka T; Harth W; McBride OW; Compton JG; Bale SJ; DiGiovanna JJ
    J Invest Dermatol; 1994 Nov; 103(5):665-8. PubMed ID: 7963653
    [TBL] [Abstract][Full Text] [Related]  

  • 34. The gene for schnyder's crystalline corneal dystrophy maps to human chromosome 1p34.1-p36.
    Shearman AM; Hudson TJ; Andresen JM; Wu X; Sohn RL; Haluska F; Housman DE; Weiss JS
    Hum Mol Genet; 1996 Oct; 5(10):1667-72. PubMed ID: 8894705
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Anterior segment mesenchymal dysgenesis: probable linkage to the MNS blood group on chromosome 4.
    Ferrell RE; Hittner HM; Kretzer FL; Antoszyk JH
    Am J Hum Genet; 1982 Mar; 34(2):245-9. PubMed ID: 6978612
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Identification of a new locus for autosomal recessive Charcot-Marie-Tooth disease with focally folded myelin on chromosome 11p15.
    Othmane KB; Johnson E; Menold M; Graham FL; Hamida MB; Hasegawa O; Rogala AD; Ohnishi A; Pericak-Vance M; Hentati F; Vance JM
    Genomics; 1999 Dec; 62(3):344-9. PubMed ID: 10644431
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Digenic inheritance of an autosomal recessive hypotrichosis in two consanguineous pedigrees.
    Basit S; Wali A; Aziz A; Muhammad N; Jelani M; Ahmad W
    Clin Genet; 2011 Mar; 79(3):273-81. PubMed ID: 20528890
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Further information regarding KERA and recessive cornea plana.
    Khan AO
    Arch Ophthalmol; 2006 Sep; 124(9):1371-2; author reply 1372. PubMed ID: 16966646
    [No Abstract]   [Full Text] [Related]  

  • 39. Genome-wide linkage and haplotype sharing analysis implicates the MCDR3 locus as a candidate region for a developmental macular disorder in association with digit abnormalities.
    Cipriani V; Kalhoro A; Arno G; Silva RS; Pontikos N; Puech V; McClements ME; Hunt DM; van Heyningen V; Michaelides M; Webster AR; Moore AT; Puech B
    Ophthalmic Genet; 2017 Dec; 38(6):511-519. PubMed ID: 28635424
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Autosomal dominant aplasia cutis congenita: report of a large Italian family and no hint for candidate chromosomal regions.
    Fimiani M; Seri M; Rubegni P; Cusano R; De Aloe G; Forabosco P; Devoto M; Andreassi L; Renieri A
    Arch Dermatol Res; 1999 Dec; 291(12):637-42. PubMed ID: 10651164
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.