109 related articles for article (PubMed ID: 17556078)
1. Deletion 9q in a patient with concomitant myelodysplasia and non-Hodgkin lymphoma.
Gozzetti A; Calabrese S; Crupi R; Tozzuoli D; Fabbri A; Bocchia M; Pirrotta MT; Defina M; Lauria F
Cancer Genet Cytogenet; 2007 Jun; 175(2):177. PubMed ID: 17556078
[No Abstract] [Full Text] [Related]
2. Isolated interstitial 9q deletion in a case of unclassifiable myelodysplastic syndrome.
Feitosa Pinheiro R; Maranhão Bahia D; Artur Flores Pelloso L; Guimaraes Vaz De Campos M; De Lourdes Chauffaille M
Cancer Genet Cytogenet; 2004 Sep; 153(2):183-4. PubMed ID: 15350312
[No Abstract] [Full Text] [Related]
3. Array comparative genomic hybridization reveals a very high frequency of deletions of the long arm of chromosome 6 in testicular lymphoma.
Bosga-Bouwer AG; Kok K; Booman M; Boven L; van der Vlies P; van den Berg A; van den Berg E; de Jong B; Poppema S; Kluin P
Genes Chromosomes Cancer; 2006 Oct; 45(10):976-81. PubMed ID: 16865685
[TBL] [Abstract][Full Text] [Related]
4. [Myelodysplasia with chromosome 7 deletion associated to tuberculosis and hepatitis C: a pattern of immunodepression synergism?].
Olave Rubio MT; Iturbe Hernández T; Arruga Manzano A; Sola Lapeña JC; Palomera Bernal L
An Med Interna; 2001 Dec; 18(12):657-8. PubMed ID: 11852506
[No Abstract] [Full Text] [Related]
5. [Autoimmune thrombocytopenia in the clinical context of myelodysplasia with chromosome 7 deletion, intestinal tuberculosis, and chronic hepatitis caused by hepatitis C virus].
Olave MT; Iturbe T; Fuertes MA; Palomera L
Sangre (Barc); 1999 Dec; 44(6):495-6. PubMed ID: 10822772
[No Abstract] [Full Text] [Related]
6. Acquired erythropoietic protoporphyria as a result of myelodysplasia causing loss of chromosome 18.
Sarkany RP; Ross G; Willis F
Br J Dermatol; 2006 Aug; 155(2):464-6. PubMed ID: 16882191
[TBL] [Abstract][Full Text] [Related]
7. [Rearrangements of chromosome 9 in different hematological neoplasia].
Andreeva SV; Drozdova VD; Ponochevnaia EV; Kavardakova NV
Tsitol Genet; 2008; 42(5):72-9. PubMed ID: 19140443
[TBL] [Abstract][Full Text] [Related]
8. Isolated deletion of 6q in a patient with myelodysplastic syndrome.
Gozzetti A; Crupi R; Defina M; Bocchia M; Raspadori D; Lauria F
Cancer Genet Cytogenet; 2009 Jul; 192(1):51. PubMed ID: 19480939
[No Abstract] [Full Text] [Related]
9. Loss of the extra chromosome 21 in a patient with Down syndrome and myelodysplasia.
Tan D; Lau LC; Teng LM; Sane S; Lim TH; Tien SL
Cancer Genet Cytogenet; 2008 Jan; 180(1):79-82. PubMed ID: 18068540
[TBL] [Abstract][Full Text] [Related]
10. Diffuse large B-cell lymphoma with TEL/ETV6 translocation.
Sevilla DW; Nandula SV; Colovai AI; Alexander S; Murty VV; Alobeid B; Bhagat G
Hum Pathol; 2009 Apr; 40(4):588-93. PubMed ID: 18992913
[TBL] [Abstract][Full Text] [Related]
11. [On the observation of a fourfold cancer].
Zimmermann G
Krebsarzt; 1969; 24(2):88-92. PubMed ID: 4895717
[No Abstract] [Full Text] [Related]
12. Lenalidomide (Revlimid) for anemia of myelodysplastic syndrome.
Med Lett Drugs Ther; 2006 Apr; 48(1232):31-2. PubMed ID: 16625140
[No Abstract] [Full Text] [Related]
13. Chromosome abnormalities and carcinogenesis.
Pogosianz HE; Prigogina EL
Neoplasma; 1972; 19(4):319-25. PubMed ID: 4262364
[No Abstract] [Full Text] [Related]
14. Familial Monosomy 7 Syndrome Associated with Myelodysplasia.
Rathi S; Kondekar S; Kadakia P; Sawardekar S; De T
Indian J Pediatr; 2019 Nov; 86(11):1059. PubMed ID: 31209763
[No Abstract] [Full Text] [Related]
15. [A particular myelodysplasia: 17p- syndrome].
Fourcade C; Jary L; Mossafa H; Louvel D
Ann Biol Clin (Paris); 1998; 56(6):724-6. PubMed ID: 9853033
[No Abstract] [Full Text] [Related]
16. 9p24 abnormalities in hematologic malignancies with a focus on diffuse large B-cell lymphoma.
Patel DA; Hahn AW; Martin MG
Med Oncol; 2017 May; 34(5):95. PubMed ID: 28409436
[No Abstract] [Full Text] [Related]
17. Isochromosome of a deleted 20q may be a relatively common abnormality in myeloid malignancies.
Ligon AH; DeAngelo DJ; Atkins L; Dal Cin P
Cancer Genet Cytogenet; 2005 Oct; 162(1):89-91. PubMed ID: 16157208
[No Abstract] [Full Text] [Related]
18. Chromosome 20 deletions in myelodysplastic syndromes and Philadelphia-chromosome-negative myeloproliferative disorders: characterization by molecular cytogenetics of commonly deleted and retained regions.
Douet-Guilbert N; Basinko A; Morel F; Le Bris MJ; Ugo V; Morice P; Berthou C; De Braekeleer M
Ann Hematol; 2008 Jul; 87(7):537-44. PubMed ID: 18350294
[TBL] [Abstract][Full Text] [Related]
19. Detailed mapping of chromosome 17p deletions reveals HIC1 as a novel tumor suppressor gene candidate telomeric to TP53 in diffuse large B-cell lymphoma.
Stöcklein H; Smardova J; Macak J; Katzenberger T; Höller S; Wessendorf S; Hutter G; Dreyling M; Haralambieva E; Mäder U; Müller-Hermelink HK; Rosenwald A; Ott G; Kalla J
Oncogene; 2008 Apr; 27(18):2613-25. PubMed ID: 17982487
[TBL] [Abstract][Full Text] [Related]
20. Myelodysplastic syndrome with isolated 5q deletion (5q- syndrome). A clonal stem cell disorder characterized by defective ribosome biogenesis.
Cazzola M
Haematologica; 2008 Jul; 93(7):967-72. PubMed ID: 18591621
[No Abstract] [Full Text] [Related]
[Next] [New Search]