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 *

92 related articles for article (PubMed ID: 9205694)

  • 21. Ophthaproblem. Vitelliform macular dystrophy (Best's disease).
    Sharma S
    Can Fam Physician; 1999 Nov; 45():2607, 2620. PubMed ID: 10587765
    [No Abstract]   [Full Text] [Related]  

  • 22. An autosomal dominant ataxia maps to 19q13: Allelic heterogeneity of SCA13 or novel locus?
    Waters MF; Fee D; Figueroa KP; Nolte D; Müller U; Advincula J; Coon H; Evidente VG; Pulst SM
    Neurology; 2005 Oct; 65(7):1111-3. PubMed ID: 16135769
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Genetics of arrhythmogenic right ventricular cardiomyopathy--status quo and future perspectives.
    Paul M; Schulze-Bahr E; Breithardt G; Wichter T
    Z Kardiol; 2003 Feb; 92(2):128-36. PubMed ID: 12596074
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A novel locus for autosomal dominant nonsyndromic hearing loss (DFNA44) maps to chromosome 3q28-29.
    Modamio-Høybjør S; Moreno-Pelayo MA; Mencía A; del Castillo I; Chardenoux S; Armenta D; Lathrop M; Petit C; Moreno F
    Hum Genet; 2003 Jan; 112(1):24-8. PubMed ID: 12483295
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Holt syndrome: an autosomal dominant, heterogeneous, acral malformation].
    Hernández Téllez A; Corona Rivera E; Martínez-Basalo C; Nazará Cazorla Z; Aguirre-Negrete MG; Cantú JM
    Bol Med Hosp Infant Mex; 1982 Feb; 39(2):131-3. PubMed ID: 7093017
    [No Abstract]   [Full Text] [Related]  

  • 26. [The genetics of Alzheimer's disease].
    Alonso-Vilatela ME; Yescas-Gómez P
    Rev Invest Clin; 1998; 50(2):155-62. PubMed ID: 9658938
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Genetic predisposition to Alzheimer's disease].
    Staufenbiel M; Pombo-Villar E
    Rev Neurol; 1997 Aug; 25(144):1285-8. PubMed ID: 9340164
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Heredity and strabismus.
    Grützner IP; Yazawa K; Spivey BE
    Surv Ophthalmol; 1970 May; 14(6):441-56. PubMed ID: 4988135
    [No Abstract]   [Full Text] [Related]  

  • 29. APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy.
    Rovelet-Lecrux A; Hannequin D; Raux G; Le Meur N; Laquerrière A; Vital A; Dumanchin C; Feuillette S; Brice A; Vercelletto M; Dubas F; Frebourg T; Campion D
    Nat Genet; 2006 Jan; 38(1):24-6. PubMed ID: 16369530
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Hereditary benign telangiectasia--first family in Northern Ireland.
    McNicholl F; McMullin MF; Nevin NC; McMillan C
    Ulster Med J; 1999 Nov; 68(2):106-7. PubMed ID: 10661639
    [No Abstract]   [Full Text] [Related]  

  • 31. Genetic aspects of supravalvular aortic stenosis.
    Morris CA
    Curr Opin Cardiol; 1998 May; 13(3):214-9. PubMed ID: 9649945
    [TBL] [Abstract][Full Text] [Related]  

  • 32. What's new in neuromuscular disorders? Nuclear envelope and Emery-Dreifuss muscular dystrophy.
    Mercuri E; Muntoni F
    Eur J Paediatr Neurol; 2001; 5(1):3-5. PubMed ID: 11277362
    [No Abstract]   [Full Text] [Related]  

  • 33. A rule concerning the segmental manifestation of autosomal dominant skin disorders. Review of clinical examples providing evidence for dichotomous types of severity.
    Happle R
    Arch Dermatol; 1997 Dec; 133(12):1505-9. PubMed ID: 9420534
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Extreme anticipation in young-onset Parkinson's disease.
    Djaldetti R; Ziv I; Melamed E
    Mov Disord; 1998 May; 13(3):599-600. PubMed ID: 9613762
    [No Abstract]   [Full Text] [Related]  

  • 35. A mild phenotype of autosomal dominant retinitis pigmentosa is associated with the rhodopsin mutation Pro-267-Leu.
    Ponjavic V; Abrahamson M; Andréasson S; Ehinger B; Fex G; Polland W
    Ophthalmic Genet; 1997 Jun; 18(2):63-70. PubMed ID: 9228242
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Genetics and Alzheimer's disease].
    Manzano S; González JL; Marcos A; Matías-Guiu J
    Neurologia; 2009 Mar; 24(2):83-9. PubMed ID: 19322684
    [TBL] [Abstract][Full Text] [Related]  

  • 37. The role of presenilin 1 in the genetics of Alzheimer's disease.
    Clark RF; Hutton M; Talbot C; Wragg M; Lendon C; Busfield F; Han SW; Perez-Tur J; Adams M; Fuldner R; Roberts G; Karran E; Hardy J; Goate A
    Cold Spring Harb Symp Quant Biol; 1996; 61():551-8. PubMed ID: 9246481
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Analysis of variation in expression of autosomal dominant osteopetrosis type 2: searching for modifier genes.
    Chu K; Koller DL; Snyder R; Fishburn T; Lai D; Waguespack SG; Foroud T; Econs MJ
    Bone; 2005 Nov; 37(5):655-61. PubMed ID: 16120485
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [de Lange syndrome].
    Ohba K
    Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):170-2. PubMed ID: 11057183
    [No Abstract]   [Full Text] [Related]  

  • 40. Molecular and cell biological aspects of Alzheimer disease.
    Shastry BS
    J Hum Genet; 2001; 46(11):609-18. PubMed ID: 11721879
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.