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8. [Nosology and diagnosis of myeloproliferative syndrome]. Zittoun R; Bernadou A; Zittoun J; Fretault J; Bousser J Sem Hop; 1968 Jun; 44(31):2079-84. PubMed ID: 4300452 [No Abstract] [Full Text] [Related]
9. [Primary and secondary thrombocythemia: apropos of 39 cases]. Bernadou A; Loo H; Prost RJ; Doumenc J; Zittoun R; Bilski-Pasquier G Sem Hop; 1968 Jun; 44(31):2092-100. PubMed ID: 4300454 [No Abstract] [Full Text] [Related]
10. Involvement of chromosomes #1 and #11 in three cases with myeloproliferative diseases. Schmid E; Köhler J Cancer Genet Cytogenet; 1984 Jan; 11(1):121-3. PubMed ID: 6580942 [TBL] [Abstract][Full Text] [Related]
11. [Familial myeloproliferative syndromes. Study of 6 families and review of literature]. Kaufman S; Brière J; Bernard J Nouv Rev Fr Hematol (1978); 1978 Apr; 20(1):1-15. PubMed ID: 353725 [TBL] [Abstract][Full Text] [Related]
12. Chromosomal abnormalities in human neoplasia. Sandberg AA; Hossfeld DK Annu Rev Med; 1970; 21():379-408. PubMed ID: 4247449 [No Abstract] [Full Text] [Related]
14. Investigations on the chromosome complement in some myeloproliferative disorders. Ponti GB; Valentini R; Carrara PM; Eridani S Acta Haematol; 1965 Jul; 34(1):36-43. PubMed ID: 4953958 [No Abstract] [Full Text] [Related]
15. Classification of chronic myeloproliferative diseases by bone marrow biopsies. Hematological and cytogenetic findings and clinical course. Georgii A; Vykoupil KF; Thiele J Bibl Haematol; 1984; (50):41-56. PubMed ID: 6590038 [No Abstract] [Full Text] [Related]
16. [Contribution of cytogenetics in the study of hemopathies]. Cadotte M Union Med Can; 1979 May; 108(5):511-4. PubMed ID: 293076 [No Abstract] [Full Text] [Related]
20. Prevalence of the frequency of JAK2 (V617F) mutation in different myeloproliferative disorders in Egyptian patients. Ebid GT; Ghareeb M; Salaheldin O; Kamel MM Int J Clin Exp Pathol; 2015; 8(9):11555-9. PubMed ID: 26617890 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]