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.
117 related articles for article (PubMed ID: 5306364)
21. [Cytogenetic studies on chronic myelocytic leukemia. Evolution of clones with additional Ph1 chromosome detected by a large number of karyotype analysis]. Tanaka K; Kamada N; Oguma N; Takimoto Y; Kuramoto A; Ohkita T Rinsho Ketsueki; 1984 Nov; 25(11):1778-87. PubMed ID: 6598207 [No Abstract] [Full Text] [Related]
22. Meaning of chromosome 6 aberrations in Ph'-positive chronic granulocytic leukemia. Palka G; Geraci L; Spadano A; Rieve AK; Betti S; Torlontano G Haematologica; 1984; 69(6):661-70. PubMed ID: 6441742 [No Abstract] [Full Text] [Related]
23. Trisomy 11 in acute phase of chronic myeloid leukemia. Philip PE Acta Haematol; 1975; 54(3):188-91. PubMed ID: 809963 [TBL] [Abstract][Full Text] [Related]
24. [Clonal analysis by fluorescence in situ hybridization in a patient with de nove acute myeloid leukemia with myelodysplasia]. Hyakuna N; Naritomi K; China K; Gushiken T; Tohma T; Ito E Rinsho Ketsueki; 1997 Sep; 38(9):776-81. PubMed ID: 9364870 [TBL] [Abstract][Full Text] [Related]
25. [Clinical significance of chromosomal abnormalities in acute non-lymphocytic leukemia (author's transl)]. Tagawa M; Sadamori N; Tomonaga Y; Kusano M; Ichimaru M; Matunaga M Rinsho Ketsueki; 1980 Jan; 21(1):1-9. PubMed ID: 6929363 [No Abstract] [Full Text] [Related]
26. [Trisomy 10p as a result of familial 10/22 translocation]. Zergollern L; Begovic D; Muzinić D Acta Med Iugosl; 1980; 34(2):113-22. PubMed ID: 7405617 [No Abstract] [Full Text] [Related]
27. [Cytogenetic study of acute leukemia]. Piatkin EK Probl Gematol Pereliv Krovi; 1966 May; 11(5):14-9. PubMed ID: 5238968 [No Abstract] [Full Text] [Related]
29. Clonal evolution in acute promyelocytic leukemia. Young GA; Singh S; Vincent PC Cancer Genet Cytogenet; 1985 Apr; 16(4):349-51. PubMed ID: 3856471 [No Abstract] [Full Text] [Related]
30. [Observation of 7 cases of rare autosomal pathology. Trisomy 9p; monosomy 18q; ring 21; trisomy 6p; trisomy 2q 1-21 translocation]. Fioretti G; Pagano L; Renda S; Festa B; Rinaldi A; Celona A; Casullo C; Stabile M; Cavaliere ML; Ventruto V Minerva Pediatr; 1980 Jun; 32(12):807-14. PubMed ID: 7464734 [No Abstract] [Full Text] [Related]
31. Trisomy 8 in bone marrow cells of a patient with erythroleukaemia. Scolozzi R; Antonelli T; Del Carmen Garcia de Luna Orozco M Haematologica; 1979 Feb; 64(1):85-9. PubMed ID: 109369 [No Abstract] [Full Text] [Related]
32. Partial trisomy of chromosome 3(p14----p22) due to maternal insertional translocation. Kleczkowska A; Fryns JP; Van den Berghe H Ann Genet; 1984; 27(3):180-3. PubMed ID: 6334484 [No Abstract] [Full Text] [Related]
33. Partial monosomy 22pter leads to q11 in a newborn with the clinical features of trisomy 13 syndrome. Back E; Stier R; Böhm N; Adlung A; Hameister H Ann Genet; 1980; 23(4):244-8. PubMed ID: 6971606 [TBL] [Abstract][Full Text] [Related]
34. [Histochemical studies on the Di Guglielmo syndrome]. Szederkényi G; Józsa L Folia Haematol Int Mag Klin Morphol Blutforsch; 1967; 88(4):218-29. PubMed ID: 4173889 [No Abstract] [Full Text] [Related]