PM Kroisel

Mental retardation in a girl with a subtelomeric deletion on chromosome 20q and complete deletion of the <i>myelin transcription factor 1</i> gene (<i>MYT1</i>)

T Kroepfl, Erwin Petek, Thomas Schwarzbraun et al. · Clinical Genetics · 2008 · 59 citations

Localization&lt;footref rid="foot01"&gt;&lt;sup&gt;1&lt;/sup&gt;&lt;/footref&gt; of the human anterior gradient-2 gene (AGR2) to chromosome band 7p21.3 by radiation hybrid mapping and fluorescencein situ hybridisation

Erwin Petek, Christian Windpassinger, H. Egger et al. · Cytogenetic and Genome Research · 2000 · 32 citations

Chromatin, Fluorescencein Situ Hybridisation, Chromosome Dynamics +14

Microdissection of a human marker chromosome reveals its origin and a new family of centromeric repetitive DNA

Daniel Johnson, PM Kroisel, Helene Klapper et al. · Human Molecular Genetics · 1992 · 28 citations

Dna, Cytogenetics, Comparative Genomics +22

Characterisation of a 19-year-old "long-term survivor" with Edwards syndrome.

Erwin Petek, Barbara Pertl, M Tschernigg et al. · PubMed · 2003 · 21 citations

Down Syndrome, Developmental Anomaly, Extra Chromosome 18 +15

Molecular characterization of a unique <i>de novo</i> 15q deletion associated with Prader–Willi syndrome and central visual impairment

Christian Windpassinger, Erwin Petek, Klaus Wagner et al. · Clinical Genetics · 2003 · 17 citations