** = Publikationen gelistet in SCI/SSCI/Pubmed
** Petek, E; Pertl, B; Tschernigg, M; Bauer, M; Mayr, J; Wagner, K; Kroisel, PM
Characterisation of a 19-year-old long-term survivor with Edwards syndrome.
Genet Couns. 2003; 14(2):239-244
(- Case Report)
Web of Science
PubMed
** Tschernigg, M; Petek, E; Leonhardtsberger, A; Wagner, K; Kroisel, PM
Terminal tandem duplication of 16p: a case with pure partial trisomy (16)(pter-->p13).
Genet Couns. 2002; 13(3):303-307
(- Case Report)
Web of Science
PubMed
** Tschernigg, M; Petek, E; Wagner, K; Kroisel, PM
Mild phenotype due to inverse duplication 4p16.3 - P15.3 including the Wolf-Hirschhorn critical region.
Genet Couns. 2002; 13(1):29-33
(- Case Report)
Web of Science
PubMed
** Emberger, W; Behmel, A; Tschernigg, M; Seewann, HL; Petek, E; Kroisel, PM; Wagner, K
Chronic myeloid leukemia with a rare variant Philadelphia translocation: t(9;10;22)(q34;q22;q11).
Cancer Genet Cytogenet. 2001; 129(1):76-79
Doi: 10.1016/S0165-4608(01)00417-4
(- Case Report)
Web of Science
PubMed
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