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

87 related items for PubMed ID: 4261193

  • 1. Cytogenic observations in congenital familial panmyelopathy (Fanconi's syndrome).
    Coutinho V, Falcao RP, Bottura C.
    Nouv Rev Fr Hematol; 1971; 11(5):781-90. PubMed ID: 4261193
    [No Abstract] [Full Text] [Related]

  • 2. [Fanconi's panmyelopathy].
    Farkas EE, Hadnagy C, Pap-Tuka P.
    Arch Kinderheilkd; 1971 Nov; 183(4):306-15. PubMed ID: 5126854
    [No Abstract] [Full Text] [Related]

  • 3. [Cytogenic and biochemical studies of 8 cases of Fanconi's anemia].
    de Grouchy J, de Nava C, Marchand JC, Feingold J, Turleau C.
    Ann Genet; 1972 Mar; 15(1):29-40. PubMed ID: 4537612
    [No Abstract] [Full Text] [Related]

  • 4. Fanconi's anaemia in an African.
    Whitehall J.
    Cent Afr J Med; 1971 Feb; 17(2):25-30. PubMed ID: 5089986
    [No Abstract] [Full Text] [Related]

  • 5. [Cytogenetic study of a case of Fanconi's syndrome with a familial pericentric inversion].
    Crippa L, Ferrier S.
    J Genet Hum; 1975 Mar; 23(1):7-16. PubMed ID: 1165481
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. [Chromosome abnormalities in bone marrow cells and peripheral lymphocytes in a patient with Fanconi's anemia].
    Margiotta G, Barbata G, Carbone P, Granata G, Caronia F.
    Minerva Med; 1981 Sep 22; 72(35):2361-5. PubMed ID: 7279258
    [Abstract] [Full Text] [Related]

  • 8. Panmyelopathy with congenital anomalies (Fanconi) in two cousins.
    Hoefnagel D, Sullivan M, McIntyre OR, Gray JA, Storrs RC.
    Helv Paediatr Acta; 1966 Jul 22; 21(3):230-8. PubMed ID: 5990992
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. A boy with congenital malformations and chromosome breakage.
    Daneshbod-Skibba G, Therman E, Shahidi NT.
    Am J Med Genet; 1980 Jul 22; 5(3):315-20. PubMed ID: 7405963
    [Abstract] [Full Text] [Related]

  • 13. Familial hypoplastic anemia with multiple congenital anomalies (Fanconi's syndrome)--report of three cases. Cases presented are of two sisters and a female cousin with complete clinical and post mortem findings.
    Esparza A, Thompson WR.
    R I Med J; 1966 Feb 22; 49(2):103-10. PubMed ID: 5217141
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. [Cytogenetic finding and etiology of Fanconi's anemia. A case of Fanconi's anemia without hexokinase deficiency].
    Schroeder TM.
    Humangenetik; 1966 Feb 22; 3(1):76-81. PubMed ID: 5986057
    [No Abstract] [Full Text] [Related]

  • 17. [Chromosome changes in Fanconi's anemia (FA) and clinical course of the disease (familial constitutional panmyelopathy)].
    Traczyk Z, Rostkowska J, Kolakowski L.
    Pol Tyg Lek; 1972 Nov 06; 27(45):1758-61. PubMed ID: 4636501
    [No Abstract] [Full Text] [Related]

  • 18. Chromosome studies in acute leukaemia. 3. Chromosome constitution of bone marrow cells in 30 cases.
    Jensen MK.
    Acta Med Scand; 1967 Nov 06; 182(5):629-44. PubMed ID: 5234257
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 5.