Duba HC - Search Results

1

Polychemotherapy combined with G-CSF-mobilized donor buffy coat transfusion for granulocytic sarcoma after allogeneic BMT for AML.

Nachbaur D, Duba HC, Feichtinger H, Kropshofer G, Nussbaumer W, Schwaighofer H, Niederwieser D. Nachbaur D, et al. Among authors: duba hc. Bone Marrow Transplant. 1997 May;19(9):947-9. doi: 10.1038/sj.bmt.1700766. Bone Marrow Transplant. 1997. PMID: 9156272

2

Chromosomal instability in a woman with infertility and two unaffected brothers: a new familial chromosomal breakage syndrome?

Duba HC, Weirich HG, Weirich-Schwaiger H, Utermann B, Nachbaur D, Sölder E, Utermann G. Duba HC, et al. Hum Genet. 1997 Sep;100(3-4):431-40. doi: 10.1007/s004390050529. Hum Genet. 1997. PMID: 9272168

3

Hepatosplenic gammadelta-T-cell lymphoma with leukemic course after renal transplantation.

Steurer M, Stauder R, Grünewald K, Gunsilius E, Duba HC, Gastl G, Dirnhofer S. Steurer M, et al. Among authors: duba hc. Hum Pathol. 2002 Feb;33(2):253-8. doi: 10.1053/hupa.2002.31301. Hum Pathol. 2002. PMID: 11957154

4

Fluorescence in situ hybridization (FISH) on peripheral blood smears for monitoring Philadelphia chromosome-positive chronic myeloid leukemia (CML) during interferon treatment: a new strategy for remission assessment.

Mühlmann J, Thaler J, Hilbe W, Bechter O, Erdel M, Utermann G, Duba HC. Mühlmann J, et al. Among authors: duba hc. Genes Chromosomes Cancer. 1998 Feb;21(2):90-100. doi: 10.1002/(sici)1098-2264(199802)21:2<90::aid-gcc3>3.0.co;2-2. Genes Chromosomes Cancer. 1998. PMID: 9491319

5

Hypermetaphase and interphase fluorescence in situ hybridisation for monitoring of remission status in Philadelphia chromosome positive chronic myeloid leukaemia.

Duba HC, Hilbe W, Mehringer A, Erdel M, Thaler J, Utermann G. Duba HC, et al. Int J Oncol. 2000 Dec;17(6):1245-9. doi: 10.3892/ijo.17.6.1245. Int J Oncol. 2000. PMID: 11078812

6

Routine screening for microdeletions by FISH in 77 patients suspected of having Prader-Willi or Angelman syndromes using YAC clone 273A2 (D15S10).

Erdel M, Schuffenhauer S, Buchholz B, Barth-Witte U, Köchl S, Utermann B, Duba HC, Utermann G. Erdel M, et al. Among authors: duba hc. Hum Genet. 1996 Jun;97(6):784-93. doi: 10.1007/BF02346190. Hum Genet. 1996. PMID: 8641697

7

The elastin gene is disrupted in a family with a balanced translocation t(7;16)(q11.23;q13) associated with a variable expression of the Williams-Beuren syndrome.

Duba HC, Doll A, Neyer M, Erdel M, Mann C, Hammerer I, Utermann G, Grzeschik KH. Duba HC, et al. Eur J Hum Genet. 2002 Jun;10(6):351-61. doi: 10.1038/sj.ejhg.5200812. Eur J Hum Genet. 2002. PMID: 12080386

8

Detection of a de novo duplication of 1q32-qter by fluorescence in situ hybridisation in a boy with multiple malformations: further delineation of the trisomy 1q syndrome.

Duba HC, Erdel M, Löffler J, Bereuther L, Fischer H, Utermann B, Utermann G. Duba HC, et al. J Med Genet. 1997 Apr;34(4):309-13. doi: 10.1136/jmg.34.4.309. J Med Genet. 1997. PMID: 9138155 Free PMC article.

9

Comparative genomic hybridization reveals a partial de novo trisomy 6q23-qter in an infant with congenital malformations: delineation of the phenotype.

Erdel M, Duba HC, Verdorfer I, Lingenhel A, Geiger R, Gutenberger KH, Ludescher E, Utermann B, Utermann G. Erdel M, et al. Among authors: duba hc. Hum Genet. 1997 May;99(5):596-601. doi: 10.1007/s004390050412. Hum Genet. 1997. PMID: 9150724

10

Nail patella syndrome in a cytogenetically balanced t(9;17)(q34.1;q25) carrier.

Duba HC, Erdel M, Löffler J, Wirth J, Utermann B, Utermann G. Duba HC, et al. Eur J Hum Genet. 1998 Jan;6(1):75-9. doi: 10.1038/sj.ejhg.5200155. Eur J Hum Genet. 1998. PMID: 9781017

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