Publications
- A double-man syndrome (48, XXYY) diagnosed in a 10-year old boy2020 | Faculty of Medicine in Pilsen
- A doubleman syndrome (48, XXYY) diagnosed in a 10-year old boy2020 | Faculty of Medicine in Pilsen
- Late diagnosis of complete androgen insensitivity syndrome and transmission/carriers of the condition in a family with mutation c.2495G. T p.(Arg832Leu) in exon 7 of the androgen receptor gene: genetic, clinical and ethical aspects2019 | Faculty of Medicine in Pilsen, Second Faculty of Medicine
- Precise determination of primary cytogenetic abnormalities provides added value for stratification of chronic lymphocytic leukemia patients2019 | Faculty of Medicine in Pilsen
- Growth disorders due to rearrangement of SHOX gene locus2019 | Faculty of Medicine in Pilsen
- Léri-Weill Syndrome on the Principle of Structural Aberration of Chromosome Y (Case Report)2018 | Faculty of Medicine in Pilsen
- Role of cytogenetic analysis in current management of childhood acute lymphoblastic leukemia treatment2015 | Faculty of Medicine in Pilsen
- Role of cytogenetic analysis in current management of childhood acute lymphoblastic leukemia treatment [Postavení cytogenetického vyšetrení v soucasném managementu lécby detské akutní lymfoblastické leukemie]2015 | Faculty of Medicine in Pilsen
- Growth disorder in a Vietnamese girl with Turner syndrome and with an uncommon cytogenetic finding2014 | Faculty of Medicine in Pilsen, First Faculty of Medicine
- Surprising diagnosis of a rare endocrine disease when examining a child for short stature2014 | Faculty of Medicine in Pilsen
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