Microdeletion and Microduplication Syndromes

Por Weise, Anja, Mrasek, Kristin, Klein, Elisabeth, Mulatinho, Milene, Llerena, Juan C., Hardekopf, David, Pekova, Sona, Bhatt, Samarth, Kosyakova, Nadezda, Liehr, Thomas
Publicado em 2012

Severe intellectual disability, omphalocele, hypospadia and high blood pressure associated to a deletion at 2q22.1q22.3: case report

Por Mulatinho, Milene Vianna, de Carvalho Serao, Cassio Luiz, Scalco, Fernanda, Hardekopf, David, Pekova, Sona, Mrasek, Kristin, Liehr, Thomas, Weise, Anja, Rao, Nagesh, Llerena, Juan Clinton
Publicado em 2012

Molecular characterization of the rare translocation t(3;10)(q26;q21) in an acute myeloid leukemia patient

Por Jancuskova, Tereza, Plachy, Radek, Zemankova, Lucie, Hardekopf, David Warren, Stika, Jiri, Zejskova, Lenka, Praulich, Inka, Kreuzer, Karl-Anton, Rothe, Achim, Othman, Moneeb AK, Kosyakova, Nadezda, Pekova, Sona
Publicado em 2014