Deletion of 14.7 Mb 2q32.3q33.3 with a marfanoid phenotype and hypothyroidismAgnieszka Tomaszewska, Malgorzata I. Srebniak, Agnieszka Podbiol‐Palenta et al.|American Journal of Medical Genetics Part A|2013Cited by 51
11p15 duplication and 13q34 deletion with <scp>B</scp>eckwith–<scp>W</scp>iedemann syndrome and factor <scp>VII</scp> deficiencyDorota Jurkiewicz, Małgorzata Krajewska‐Walasek, Agata Cieślikowska et al.|Pediatrics International|2015Cited by 5
The first de novo non‐mosaic 14q11.2q13.1 tetrasomy of paternal originAgnieszka Tomaszewska, Malgorzata I. Srebniak, Robert‐Jan H. Galjaard et al.|American Journal of Medical Genetics Part A|2016Cited by 0