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H C Duba

Showing results (21-30 of 32) with videos related to

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Reproductive Biomedicine Online|July 17, 2012
Planar embryos have poor prognosis in terms of blastocyst formation and implantationT Ebner, M Maurer, O Shebl, et al.
Klinische Padiatrie|May 1, 1993
Constitutional interstitial deletion of 17(p11.2) (Smith-Magenis syndrome): a clinically recognizable microdeletion syndrome. Report of two cases and review of the literatureH Fischer, H P Oswald, H C Duba, et al.
Human Genetics|September 1, 1997
Chromosomal instability in a woman with infertility and two unaffected brothers: a new familial chromosomal breakage syndrome?H C Duba, H G Weirich, H Weirich-Schwaiger, et al.
International Journal of Oncology|December 24, 1998
Monitoring of remission status by fluorescence in situ hybridisation in chronic myeloid leukaemia patients treated with interferon-alphaH C Duba, S Peter, W Hilbe, et al.
International Journal of Oncology|November 20, 2001
Combined study of prostatic carcinoma by classical cytogenetic analysis and comparative genomic hybridizationI Verdorfer, A Hobisch, Z Culig, et al.
Human Genetics|June 1, 1996
Routine screening for microdeletions by FISH in 77 patients suspected of having Prader-Willi or Angelman syndromes using YAC clone 273A2 (D15S10)M Erdel, S Schuffenhauer, B Buchholz, et al.
Annals of Hematology|September 1, 2001
Spontaneous remission in a secondary acute myelogenous leukaemia following invasive pulmonary aspergillosisA Tzankov, C Ludescher, H C Duba, et al.
Human Genetics|May 1, 1997
Comparative genomic hybridization reveals a partial de novo trisomy 6q23-qter in an infant with congenital malformations: delineation of the phenotypeM Erdel, H C Duba, I Verdorfer, et al.
Lancet (London, England)|July 25, 2000
Evidence from a leukaemia model for maintenance of vascular endothelium by bone-marrow-derived endothelial cellsE Gunsilius, H C Duba, A L Petzer, et al.
Annals of Human Genetics|November 27, 2015
New Mutations Associated with Rasopathies in a Central European Population and Genotype-Phenotype CorrelationsM Čizmárová, K Hlinková, S Bertok, et al.
Pageof 4

Showing results (21-30 of 32) with videos related to

Sort By:
Pageof 4
Reproductive Biomedicine Online|July 17, 2012
Planar embryos have poor prognosis in terms of blastocyst formation and implantationT Ebner, M Maurer, O Shebl, et al.
Klinische Padiatrie|May 1, 1993
Constitutional interstitial deletion of 17(p11.2) (Smith-Magenis syndrome): a clinically recognizable microdeletion syndrome. Report of two cases and review of the literatureH Fischer, H P Oswald, H C Duba, et al.
Human Genetics|September 1, 1997
Chromosomal instability in a woman with infertility and two unaffected brothers: a new familial chromosomal breakage syndrome?H C Duba, H G Weirich, H Weirich-Schwaiger, et al.
International Journal of Oncology|December 24, 1998
Monitoring of remission status by fluorescence in situ hybridisation in chronic myeloid leukaemia patients treated with interferon-alphaH C Duba, S Peter, W Hilbe, et al.
International Journal of Oncology|November 20, 2001
Combined study of prostatic carcinoma by classical cytogenetic analysis and comparative genomic hybridizationI Verdorfer, A Hobisch, Z Culig, et al.
Human Genetics|June 1, 1996
Routine screening for microdeletions by FISH in 77 patients suspected of having Prader-Willi or Angelman syndromes using YAC clone 273A2 (D15S10)M Erdel, S Schuffenhauer, B Buchholz, et al.
Annals of Hematology|September 1, 2001
Spontaneous remission in a secondary acute myelogenous leukaemia following invasive pulmonary aspergillosisA Tzankov, C Ludescher, H C Duba, et al.
Human Genetics|May 1, 1997
Comparative genomic hybridization reveals a partial de novo trisomy 6q23-qter in an infant with congenital malformations: delineation of the phenotypeM Erdel, H C Duba, I Verdorfer, et al.
Lancet (London, England)|July 25, 2000
Evidence from a leukaemia model for maintenance of vascular endothelium by bone-marrow-derived endothelial cellsE Gunsilius, H C Duba, A L Petzer, et al.
Annals of Human Genetics|November 27, 2015
New Mutations Associated with Rasopathies in a Central European Population and Genotype-Phenotype CorrelationsM Čizmárová, K Hlinková, S Bertok, et al.
Pageof 4