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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

104 related items for PubMed ID: 483445

  • 41. Chromosomal instability in hereditary tyrosinemia type I.
    Wilson KS, Timmons CF, Hilton DS, Weinberg AG, Tonk V.
    Pediatr Pathol; 1994; 14(6):1055-7. PubMed ID: 7855008
    [No Abstract] [Full Text] [Related]

  • 42.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 43.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 44.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 45.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 46. Simple detection of a (Finnish) hereditary tyrosinemia type 1 mutation.
    St-Louis M, Poudrier J, Tanguay RM.
    Hum Mutat; 1996; 7(4):379-80. PubMed ID: 8723698
    [No Abstract] [Full Text] [Related]

  • 47.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 48.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 49.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 50. [Disorders in the tyrosine metabolism. II. Tyrosinemia - a congenital metabolic disorder].
    Vulović D, Hajduković R, Sindjić M, FilipovićD, Dozić S.
    Srp Arh Celok Lek; 1974 Jan; 102(1):9-20. PubMed ID: 4368107
    [No Abstract] [Full Text] [Related]

  • 51.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 52.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 53. Hereditary tyrosinemia: unusual imaging distribution of gallium-67 citrate.
    Malinoff HL, Mountz JM, Wilson MW.
    Clin Nucl Med; 1989 Mar; 14(3):229. PubMed ID: 2736851
    [No Abstract] [Full Text] [Related]

  • 54. Six novel mutations in the fumarylacetoacetate hydrolase gene of patients with hereditary tyrosinemia type I.
    Timmers C, Grompe M.
    Hum Mutat; 1996 Mar; 7(4):367-9. PubMed ID: 8723690
    [No Abstract] [Full Text] [Related]

  • 55.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 56. [A rare cause of neonatal hyperphenylalaninemia: tyrosinemia type I].
    Sarles J, Maurin N, Giraud F.
    Pediatrie; 1992 Mar; 47(12):809-11. PubMed ID: 1338924
    [Abstract] [Full Text] [Related]

  • 57. Hereditary tyrosinemia in a French Canadian isolate.
    Laberge C.
    Am J Hum Genet; 1969 Jan; 21(1):36-45. PubMed ID: 5763606
    [No Abstract] [Full Text] [Related]

  • 58.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 59. Hereditary tyrosinemia in the province of Quebec: prevalence at birth and geographic distribution.
    Bergeron P, Laberge C, Grenier A.
    Clin Genet; 1974 Jan; 5(2):157-62. PubMed ID: 4829425
    [No Abstract] [Full Text] [Related]

  • 60. The occurrence of hepatoma in the chronic form of hereditary tyrosinemia.
    Weinberg AG, Mize CE, Worthen HG.
    J Pediatr; 1976 Mar; 88(3):434-8. PubMed ID: 173827
    [Abstract] [Full Text] [Related]

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