BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

169 related articles for article (PubMed ID: 4983623)

  • 1. Autosomal recessive oculocutaneous albinism in man. Evidence for genetic heterogeneity.
    Witkop CJ; Nance WE; Rawls RF; White JG
    Am J Hum Genet; 1970 Jan; 22(1):55-74. PubMed ID: 4983623
    [No Abstract]   [Full Text] [Related]  

  • 2. Albinism.
    Witkop CJ
    Adv Hum Genet; 1971; 2():61-142. PubMed ID: 5005925
    [No Abstract]   [Full Text] [Related]  

  • 3. Human albinism.
    Jay B; Carruthers J; Treplin MC; Winder AF
    Birth Defects Orig Artic Ser; 1976; 12(3):415-26. PubMed ID: 821563
    [No Abstract]   [Full Text] [Related]  

  • 4. [Oculo-cutaneous albinism in man. Biochemical, genetic, clinical, and population aspects].
    Cassero C; Montana R
    Arch Sci Med (Torino); 1983; 140(2):105-26. PubMed ID: 6882187
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genetic and metabolic bases of two "albino" phenotypes in the leopard frog, Rana pipiens.
    Smith-Gill SJ; Richards CM; Nace GW
    J Exp Zool; 1972 May; 180(2):157-67. PubMed ID: 4623610
    [No Abstract]   [Full Text] [Related]  

  • 6. Segregation analysis of brown oculocutaneous albinism.
    King RA; Rich SS
    Clin Genet; 1986 Jun; 29(6):496-501. PubMed ID: 3742854
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mutation analysis of the tyrosinase gene in oculocutaneous albinism.
    Camand O; Marchant D; Boutboul S; PĂ©quignot M; Odent S; Dollfus H; Sutherland J; Levin A; Menasche M; Marsac C; Dufier JL; Heon E; Abitbol M
    Hum Mutat; 2001 Apr; 17(4):352. PubMed ID: 11295837
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Experimental studies on a mutant gene, a, causing albinism in the axolotl, Ambystoma mexicanum.
    Harsa-King ML
    Dev Biol; 1978 Feb; 62(2):370-88. PubMed ID: 414944
    [No Abstract]   [Full Text] [Related]  

  • 9. Hairbulb tyrosinase activity in oculocutaneous albinism: suggestions for pathway control and block location.
    King RA; Olds DP
    Am J Med Genet; 1985 Jan; 20(1):49-55. PubMed ID: 3918447
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetic and biochemical evidence for two forms of oculocutaneous albinism in man.
    Nance WE; Witkop CJ; Rawls RF
    Birth Defects Orig Artic Ser; 1971 Mar; 7(3):125-8. PubMed ID: 5173133
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Hairbulb tyrosinase activity in oculocutaneous albinism.
    King RA; Witkop CJ
    Nature; 1976 Sep; 263(5572):69-71. PubMed ID: 822352
    [No Abstract]   [Full Text] [Related]  

  • 12. Tyrosinase positive oculocutaneous albinism among the Zuni and the Brandywine triracial isolate: biochemical and clinical characteristics and fertility.
    Witkop CJ; Niswander JD; Bergsma DR; Workman PL; White JG
    Am J Phys Anthropol; 1972 May; 36(3):397-405. PubMed ID: 4624656
    [No Abstract]   [Full Text] [Related]  

  • 13. A frequent tyrosinase gene mutation in classic, tyrosinase-negative (type IA) oculocutaneous albinism.
    Giebel LB; Strunk KM; King RA; Hanifin JM; Spritz RA
    Proc Natl Acad Sci U S A; 1990 May; 87(9):3255-8. PubMed ID: 1970634
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Albinism in Nigeria with delineation of new recessive oculocutaneous type.
    King RA; Creel D; Cervenka J; Okoro AN; Witkop CJ
    Clin Genet; 1980 Apr; 17(4):259-70. PubMed ID: 6768477
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Familial progressive hyperpigmentation.
    Chernosky ME; Anderson DE; Chang JP; Shaw MW; Romsdahl MM
    Arch Dermatol; 1971 Jun; 103(6):581-91 passim. PubMed ID: 4326548
    [No Abstract]   [Full Text] [Related]  

  • 16. Hereditary puzzles in albinism: heterogeneity or phenotypical variation?
    Taylor WO
    Trans Ophthalmol Soc U K (1962); 1983; 103 ( Pt 3)():318-30. PubMed ID: 6585074
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Hopi indians, inbreeding, and albinism.
    Woolf CM; Dukepoo FC
    Science; 1969 Apr; 164(3875):30-7. PubMed ID: 5773710
    [No Abstract]   [Full Text] [Related]  

  • 18. Investigation of a case of oculocutaneous albinism.
    Jung EG; Anton-Lamprecht I
    Birth Defects Orig Artic Ser; 1971 Jun; 7(8):26-30. PubMed ID: 5006146
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mutations of the P gene in oculocutaneous albinism, ocular albinism, and Prader-Willi syndrome plus albinism.
    Lee ST; Nicholls RD; Bundey S; Laxova R; Musarella M; Spritz RA
    N Engl J Med; 1994 Feb; 330(8):529-34. PubMed ID: 8302318
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Albinism, or the NOACH syndrome (the book of Enoch c.v. 1-20).
    van Dorp DB
    Clin Genet; 1987 Apr; 31(4):228-42. PubMed ID: 3109790
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.