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Gene mutations connected to Waldenstöm macroglobulinemia

Vnitřní lékar̆stvĭ, 2016-01, Vol.62 (1), p.40-43

2016

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Analysis of cell free fetal DNA fragmentation rate in pregnant women during the course of gravidit

Ceská gynekologie, 2010-08, Vol.75 (4), p.312

2010

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Practical aspects and clinical value of t(14;18) monitoring in peripheral blood of the follicular lymphoma patients

Časopis lékařů českých, 2007, Vol.146 (4), p.374-81; discussion 381-2

2007

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News in diagnostics and therapy of multiple endocrine neoplasia type 1

Vnitřní lékar̆stvĭ, 2015-10, Vol.61 (10), p.896-899

Starý, Karel

2015

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Extracellular chromosome 21--derived microRNAs in maternal circulation: evaluation of their diagnostic potential for screening of Down syndrome

Ceská gynekologie, 2012-10, Vol.77 (5), p.395

2012

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Dilemma of the results interpretation of molecular genetic analysis with a focus on CFTR gene mutations in men with reproductive disorders and in gamete donors

Ceská gynekologie, 2008-12, Vol.73 (6), p.323

Hrdlicka, I

2008

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Noninvasive fetal sex detection from maternal plasma in pregnant women

Ceská gynekologie, 2008-06, Vol.73 (3), p.150

2008

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The molecular genetic assessment of prognostic factors in carcioma of the prostate: a pilot study

Ceskoslovenské patologie, 2006-07, Vol.42 (3), p.130-132

2006

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Choroid plexus cysts and risk of trisomy 18. Modifications regarding maternal age and markers

Ceská gynekologie, 2007-01, Vol.72 (1), p.49

2007

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Comparison of standard prognostic factors with the deletion of 13q14 detected by interphase fluorescence in situ hybridization on separated and unseparated bone marrow cells in multiple myeloma

Časopis lékařů českých, 2005, Vol.144 (7), p.483-488

2005

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Rearrangements of 11q in patients with hematologic malignancies

Časopis lékařů českých, 2002-09, Vol.141 Suppl, p.38

2002

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Invasive ductal carcinoma of the breast: study of the number of copies of the CCND1 gene and chromosome 11 using fluorescence in situ hybridization (FISH) in comparison with expression of cyclin D1 protein and estrogen receptors (ER alpha) with immunohistochemical detection

Časopis lékařů českých, 2002-11, Vol.141 (22), p.708

2002

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PCR-multiplex system for analysis of Y-chromosomal microsatellite polymorphisms DYS449, DYS456, DYS458, and DYS464

Soudni lekarstvi, 2006-04, Vol.51 (2), p.30

2006

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Ret proto-oncogene mutation found in the Czech population and its predictive value for offspring of patients with medullary carcinoma of the thyroid gland

Vnitřní lékar̆stvĭ, 1996-11, Vol.42 (11), p.751

1996

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Leiomyomas of the uterine body: Molecular-genetical aspects of formation and development

Ceská gynekologie, 2016-01, Vol.81 (1), p.48

2016

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Lenalidomide treatment in myelodysplastic syndrome with 5q deletion--Czech MDS group experience

Vnitřní lékar̆stvĭ, 2015-12, Vol.61 (12), p.1028-1033

2015

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Diagnosis of tuberous sclerosis complex focusing on prenatal period

Ceská gynekologie, 2016-04, Vol.81 (2), p.147

2016

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Chromosome banding analysis of peripheral blood lymphocytes stimulated with IL2 and CpG oligonucleotide DSP30 in patients with chronic lymphocytic leukemia

Klinická onkologie, 2013, Vol.26 (4), p.263-270

2013

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Rapid detection of the most common chromosomal aneuploidies in the second-trimester amniotic fluid using QF-PCR

Ceská gynekologie, 2013-08, Vol.78 (4), p.373

2013

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Mutagenic effect of advanced paternal age in neurocardiofaciocutaneous syndrome

Časopis lékařů českých, 2014, Vol.153 (5), p.242

2014

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Detection of chromosome changes by CGH, array-CGH and SNP array techniques in tumours

Ceskoslovenské patologie, 2014-01, Vol.50 (1), p.25-29

2014

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

Klinická onkologie, 2014, Vol.27 (3), p.183-191

2014

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Genetic factors in etiology of uterine fibroids

Ceská gynekologie, 2012-02, Vol.77 (1), p.58

2012

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Chromosomal integration of the sixth human herpes virus (HHV-6)

Epidemiologie, mikrobiologie, imunologie, 2012-09, Vol.61 (3), p.58

2012

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First experiences with preimplantation genetic screening of chromosomal aberrations using oligonucleotide-based array comparative genomic hybridization

Časopis lékařů českých, 2015, Vol.154 (3), p.127

2015

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Gene mutations connected to Waldenstöm macroglobulinemia

Analysis of cell free fetal DNA fragmentation rate in pregnant women during the course of gravidit

Practical aspects and clinical value of t(14;18) monitoring in peripheral blood of the follicular lymphoma patients

News in diagnostics and therapy of multiple endocrine neoplasia type 1

Extracellular chromosome 21--derived microRNAs in maternal circulation: evaluation of their diagnostic potential for screening of Down syndrome

Dilemma of the results interpretation of molecular genetic analysis with a focus on CFTR gene mutations in men with reproductive disorders and in gamete donors

Noninvasive fetal sex detection from maternal plasma in pregnant women

The molecular genetic assessment of prognostic factors in carcioma of the prostate: a pilot study

Choroid plexus cysts and risk of trisomy 18. Modifications regarding maternal age and markers

Comparison of standard prognostic factors with the deletion of 13q14 detected by interphase fluorescence in situ hybridization on separated and unseparated bone marrow cells in multiple myeloma

Rearrangements of 11q in patients with hematologic malignancies

Invasive ductal carcinoma of the breast: study of the number of copies of the CCND1 gene and chromosome 11 using fluorescence in situ hybridization (FISH) in comparison with expression of cyclin D1 protein and estrogen receptors (ER alpha) with immunohistochemical detection

PCR-multiplex system for analysis of Y-chromosomal microsatellite polymorphisms DYS449, DYS456, DYS458, and DYS464

Ret proto-oncogene mutation found in the Czech population and its predictive value for offspring of patients with medullary carcinoma of the thyroid gland

Leiomyomas of the uterine body: Molecular-genetical aspects of formation and development

Lenalidomide treatment in myelodysplastic syndrome with 5q deletion--Czech MDS group experience

Diagnosis of tuberous sclerosis complex focusing on prenatal period

Chromosome banding analysis of peripheral blood lymphocytes stimulated with IL2 and CpG oligonucleotide DSP30 in patients with chronic lymphocytic leukemia

Rapid detection of the most common chromosomal aneuploidies in the second-trimester amniotic fluid using QF-PCR

Mutagenic effect of advanced paternal age in neurocardiofaciocutaneous syndrome

Detection of chromosome changes by CGH, array-CGH and SNP array techniques in tumours

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

Genetic factors in etiology of uterine fibroids

Chromosomal integration of the sixth human herpes virus (HHV-6)

First experiences with preimplantation genetic screening of chromosomal aberrations using oligonucleotide-based array comparative genomic hybridization

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