Halka Lhotska

Prague, PR 12800, Czech Republic

Last Updated: 09/26/2026

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Found 12 publications

Validating a clinically based MS-MLPA threshold through comparison with Sanger sequencing in glioblastoma patients.

Validating a clinically based MS-MLPA threshold through comparison with Sanger sequencing in glioblastoma patients.

Journal: Clinical epigenetics

Published: July 26, 2024

Diagnostic challenges in complicated case of glioblastoma.

Diagnostic challenges in complicated case of glioblastoma.

Journal: Pathology oncology research : POR

Published: June 13, 2024

Cryptic aberrations may allow more accurate prognostic classification of patients with myelodysplastic syndromes and clonal evolution.

Cryptic aberrations may allow more accurate prognostic classification of patients with myelodysplastic syndromes and clonal evolution.

Journal: Genes, chromosomes & cancer

Published: August 12, 2019

ASXL1 gene alterations in patients with isolated 20q deletion.

ASXL1 gene alterations in patients with isolated 20q deletion.

Journal: Neoplasma

Published: October 10, 2018

Mantle cell lymphoma-variant Richter syndrome: Detailed molecular-cytogenetic and backtracking analysis reveals slow evolution of a pre-MCL clone in parallel with CLL over several years.

Mantle cell lymphoma-variant Richter syndrome: Detailed molecular-cytogenetic and backtracking analysis reveals slow evolution of a pre-MCL clone in parallel with CLL over several years.

Journal: International journal of cancer

Published: March 08, 2016

Primary and recurrent diffuse astrocytomas: genomic profile comparison reveals acquisition of biologically relevant aberrations.

Primary and recurrent diffuse astrocytomas: genomic profile comparison reveals acquisition of biologically relevant aberrations.

Journal: Molecular cytogenetics

Published: November 05, 2015

Copy number neutral loss of heterozygosity at 17p and homozygous mutations of TP53 are associated with complex chromosomal aberrations in patients newly diagnosed with myelodysplastic syndromes.

Copy number neutral loss of heterozygosity at 17p and homozygous mutations of TP53 are associated with complex chromosomal aberrations in patients newly diagnosed with myelodysplastic syndromes.

Journal: Leukemia research

Published: September 22, 2015

Genetic and epigenetic characterization of low-grade gliomas reveals frequent methylation of the MLH3 gene.

Genetic and epigenetic characterization of low-grade gliomas reveals frequent methylation of the MLH3 gene.

Journal: Genes, chromosomes & cancer

Published: February 02, 2015

An unusual case of high hyperdiploid childhood ALL with cryptic BCR/ABL1 rearrangement.

An unusual case of high hyperdiploid childhood ALL with cryptic BCR/ABL1 rearrangement.

Journal: Molecular cytogenetics

Published: July 25, 2014

Molecular cytogenetic analysis of chromosomal aberrations in cells of low grade gliomas and its contribution for tumour classification

Molecular cytogenetic analysis of chromosomal aberrations in cells of low grade gliomas and its contribution for tumour classification

Journal: Klinicka onkologie : casopis Ceske a Slovenske onkologicke spolecnosti

Published: June 12, 2014

Change in ploidy status from hyperdiploid to near-tetraploid in multiple myeloma associated with bortezomib/lenalidomide resistance.

Change in ploidy status from hyperdiploid to near-tetraploid in multiple myeloma associated with bortezomib/lenalidomide resistance.

Journal: Cancer genetics

Published: February 14, 2014

Jumping-like translocation-a rare chromosomal rearrangement in a patient with Burkitt lymphoma/leukemia.

Jumping-like translocation-a rare chromosomal rearrangement in a patient with Burkitt lymphoma/leukemia.

Journal: Cancer genetics

Published: November 21, 2013

Showing 1-12 of 12

Last Updated: 09/26/2026