Seeger D - Search Results

1

3p21 is a recurrent treatment-related breakpoint in myelodysplastic syndrome and acute myeloid leukemia.

Shi G, Weh HJ, Martensen S, Seeger D, Hossfeld DK. Shi G, et al. Among authors: seeger d. Cytogenet Cell Genet. 1996;74(4):295-9. doi: 10.1159/000134439. Cytogenet Cell Genet. 1996. PMID: 8976389

2

Deletion of chromosome 15 represents a rare but recurrent chromosomal abnormality in myelocytic malignancies.

Dierlamm J, Schilling G, Michaux L, Hinz K, Murga Penas EM, Seeger D, Hagemeijer A, Hossfeld DK. Dierlamm J, et al. Among authors: seeger d. Cancer Genet Cytogenet. 2003 Jul 1;144(1):1-5. doi: 10.1016/s0165-4608(02)00863-4. Cancer Genet Cytogenet. 2003. PMID: 12810248 Review.

3

Dicentric (19;21)(p13;p13), a novel chromosomal abnormality occurring in a case of Philadelphia chromosome-positive acute lymphoblastic leukemia.

Schilling G, Dierlamm J, Murga Penas EM, Hinz K, Seeger D, Hossfeld DK. Schilling G, et al. Among authors: seeger d. Cancer Genet Cytogenet. 2004 Jul 15;152(2):129-31. doi: 10.1016/j.cancergencyto.2003.10.018. Cancer Genet Cytogenet. 2004. PMID: 15262431

4

Prognostic significance of chromosome analysis in de novo acute myeloid leukemia (AML).

Weh HJ, Kuse R, Hoffmann R, Seeger D, Suciu S, Kabisch H, Ritter J, Hossfeld DK. Weh HJ, et al. Among authors: seeger d. Blut. 1988 Jan;56(1):19-26. doi: 10.1007/BF00321055. Blut. 1988. PMID: 3422167

5

Trisomy 8 preceding diagnosis of acute nonlymphocytic leukemia by 2 years in a patient with multiple myeloma without cytological evidence of myelodysplasia.

Weh HJ, Seeger D, Junge I, Hossfeld DK. Weh HJ, et al. Among authors: seeger d. Ann Hematol. 1996 Feb;72(2):81-2. doi: 10.1007/BF00641312. Ann Hematol. 1996. PMID: 8597611

6

t(1;19)(q23;p13) in a case of acute monocytic leukemia.

Weh HJ, Jonveaux P, Seeger D, Felgner J, Hossfeld DK. Weh HJ, et al. Among authors: seeger d. Cancer Genet Cytogenet. 1996 Mar;87(1):52-4. doi: 10.1016/0165-4608(95)00238-3. Cancer Genet Cytogenet. 1996. PMID: 8646742

7

Novel Philadelphia variant t(Y;9;22)(q12;q34;q11) in a case of chronic myeloid leukemia.

Dierlamm J, Michaux L, Stefanova M, Eggert J, Leberecht P, Seeger D, Westerhausen M, Hossfeld DK. Dierlamm J, et al. Among authors: seeger d. Cancer Genet Cytogenet. 1999 Oct 15;114(2):150-3. doi: 10.1016/s0165-4608(99)00050-3. Cancer Genet Cytogenet. 1999. PMID: 10549273

8

Polysomy 13 with concomitant deletion of 13q13-14 involving the retinoblastoma gene and the D13S25 locus in a case of acute myeloid leukemia.

Stefanova M, Dierlamm J, Michaux L, Leberecht P, Seeger D, Hinz K, Hossfeld DK. Stefanova M, et al. Among authors: seeger d. Cancer Genet Cytogenet. 2000 Jun;119(2):158-61. doi: 10.1016/s0165-4608(99)00230-7. Cancer Genet Cytogenet. 2000. PMID: 10867153

9

Cytogenetic Studies in Patients with Acute Myeloid Leukemia Following a Myelodysplastic Syndrome.

Weh HJ, Kuse R, Seeger D, Suciu S, Hossfeld DK. Weh HJ, et al. Among authors: seeger d. Leuk Lymphoma. 1991;3(5-6):423-7. doi: 10.3109/10428199109070287. Leuk Lymphoma. 1991. PMID: 27467434

10

A novel cryptic translocation t(12;17)(p13;p12-p13) in a secondary acute myeloid leukemia results in a fusion of the ETV6 gene and the antisense strand of the PER1 gene.

Murga Penas EM, Cools J, Algenstaedt P, Hinz K, Seeger D, Schafhausen P, Schilling G, Marynen P, Hossfeld DK, Dierlamm J. Murga Penas EM, et al. Among authors: seeger d. Genes Chromosomes Cancer. 2003 May;37(1):79-83. doi: 10.1002/gcc.10175. Genes Chromosomes Cancer. 2003. PMID: 12661008

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