Application of the new insertion–deletion polymorphism kit for forensic identification and parentage testing on the Czech population

por Zidkova, Anastassiya, Horinek, Ales, Kebrdlova, Vera, Korabecna, Marie
Publicado 2011

Performance of Droplet Digital PCR in Non-Invasive Fetal RHD Genotyping - Comparison with a Routine Real-Time PCR Based Approach

por Svobodová, Iveta, Pazourková, Eva, Hořínek, Aleš, Novotná, Michaela, Calda, Pavel, Korabečná, Marie
Publicado 2015

Genome-wide miRNA profiling in plasma of pregnant women with down syndrome fetuses

por Zedníková, Iveta, Chylíková, Blanka, Šeda, Ondřej, Korabečná, Marie, Pazourková, Eva, Břešťák, Miroslav, Krkavcová, Miroslava, Calda, Pavel, Hořínek, Aleš
Publicado 2020

Snail Track Lesion with Flat Keratometry in Anterior Segment Dysgenesis Caused by a Novel FOXC1 Variant

por Skalicka, Pavlina, Jedlickova, Jana, Horinek, Ales, Trkova, Marie, Davidson, Alice E., Tuft, Stephen J., Dudakova, Lubica, Liskova, Petra
Publicado 2022

Schnyder corneal dystrophy and associated phenotypes caused by novel and recurrent mutations in the UBIAD1 gene

por Evans, Cerys J., Dudakova, Lubica, Skalicka, Pavlina, Mahelkova, Gabriela, Horinek, Ales, Hardcastle, Alison J., Tuft, Stephen J., Liskova, Petra
Publicado 2018