Mecucci C - Search Results

1

The short arm of chromosome 6 is nonrandomly rearranged in secondary myelodysplastic syndromes.

Mecucci C, Michaux JL, Louwagie A, Boogaerts M, Van den Berghe H. Mecucci C, et al. Cancer Genet Cytogenet. 1988 Apr;31(2):147-55. doi: 10.1016/0165-4608(88)90210-5. Cancer Genet Cytogenet. 1988. PMID: 3162388

2

Deletion of 5q by t(5;17) in therapy-related myelodysplastic syndrome.

Vandenberghe EA, Mecucci C, Delannoy A, Van den Berghe H. Vandenberghe EA, et al. Among authors: mecucci c. Cancer Genet Cytogenet. 1990 Aug 1;48(1):49-52. doi: 10.1016/0165-4608(90)90215-v. Cancer Genet Cytogenet. 1990. PMID: 2372787 No abstract available.

3

5q- anomaly in lymphoid disorders.

Kerim S, Mecucci C, Cuneo A, Vandenberghe E, Louwagie A, Stul M, Michaux JL, Van Den Berghe H. Kerim S, et al. Among authors: mecucci c. Leukemia. 1990 Jan;4(1):12-5. Leukemia. 1990. PMID: 2404161 Review.

4

Cytogenetic and clinical investigations in 76 cases with therapy-related leukemia and myelodysplastic syndrome.

Iurlo A, Mecucci C, Van Orshoven A, Michaux JL, Boogaerts M, Noens L, Bosly A, Louwagie A, Van Den Berghe H. Iurlo A, et al. Among authors: mecucci c. Cancer Genet Cytogenet. 1989 Dec;43(2):227-41. doi: 10.1016/0165-4608(89)90034-4. Cancer Genet Cytogenet. 1989. PMID: 2598167

5

Characterization of deletions of chromosome 7 short arm occurring as primary karyotypic anomaly in acute myeloid leukaemia.

Mecucci C, Van Orshoven A, Boogaerts M, Michaux JL, Van den Berghe H. Mecucci C, et al. Br J Haematol. 1989 Jan;71(1):13-7. doi: 10.1111/j.1365-2141.1989.tb06267.x. Br J Haematol. 1989. PMID: 2917120

6

6p+ and 9q- in two chromosomally distinct clones occurring in a case of myelodysplastic syndrome evolving to acute nonlymphocytic leukemia.

Ringressi A, Mecucci C, Grossi A, Bernabei PA, Ferrini PR, Van den Berghe H. Ringressi A, et al. Among authors: mecucci c. Cancer Genet Cytogenet. 1988 Oct 15;35(2):213-21. doi: 10.1016/0165-4608(88)90243-9. Cancer Genet Cytogenet. 1988. PMID: 3052797 Review.

7

Inversion (4)(p13q28) in two cases of acute nonlymphocytic leukemia.

Iurlo A, Mecucci C, Van Orshoven A, Michaux JL, Van den Berghe H. Iurlo A, et al. Among authors: mecucci c. Cancer Genet Cytogenet. 1988 Dec;36(2):143-7. doi: 10.1016/0165-4608(88)90136-7. Cancer Genet Cytogenet. 1988. PMID: 3203300

8

The karyotype in secondary hematologic disorders after treatment for Hodgkin's disease. A study of 19 patients.

Iurlo A, Mecucci C, Van Orshoven A, Michaux JL, Boogaerts M, Van den Berghe H. Iurlo A, et al. Among authors: mecucci c. Cancer Genet Cytogenet. 1988 Dec;36(2):165-72. doi: 10.1016/0165-4608(88)90140-9. Cancer Genet Cytogenet. 1988. PMID: 3203304

9

The origin of trisomy 12 in B-cell chronic lymphocytic leukemia.

Mecucci C, Delannoy A, Van den Berghe H. Mecucci C, et al. Cancer Genet Cytogenet. 1988 Dec;36(2):203-4. doi: 10.1016/0165-4608(88)90146-x. Cancer Genet Cytogenet. 1988. PMID: 3203310 No abstract available.

10

Cytogenetic studies in T-cell malignancies.

Mecucci C, Louwagie A, Thomas J, Boogaerts M, Van Den Berghe H. Mecucci C, et al. Cancer Genet Cytogenet. 1988 Jan;30(1):63-71. doi: 10.1016/0165-4608(88)90093-3. Cancer Genet Cytogenet. 1988. PMID: 3257157

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