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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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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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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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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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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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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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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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Mutagenic effect of advanced paternal age in neurocardiofaciocutaneous syndrome

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

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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Clinical relevance of chromosomal aberrations in bone and soft tissue tumors in children and young adults

Klinická onkologie, 2009, Vol.22 (2), p.58-66

2009

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Chromosome instability syndromes

Časopis lékařů českých, 2002, Vol.141 (1), p.16

2002

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Microdeletion of the azoospermia factor as one of the causes of male infertility

Časopis lékařů českých, 2003, Vol.142 (4), p.211

2003

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Molecular diagnosis of haemophilia A in clinical practice

Časopis lékařů českých, 2005, Vol.144 (12), p.795-800

Habart, D

2005

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Increased risk of malignancies in heterozygotes in families of patients with Nijmegen breakage syndrome

Časopis lékařů českých, 2006, Vol.145 (2), p.138-143

2006

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Mosaic phenotypes

Časopis lékařů českých, 2002-07, Vol.141 (14), p.439

Seemanová, E

2002

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Pericentric inversion of human chromosomes and its risks

Časopis lékařů českých, 2001-02, Vol.140 (2), p.38

Balícek, P

2001

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Chromosome markers and balanced translocation in the etiology of infertility

Ceská gynekologie, 1998-02, Vol.63 (1), p.51

1998

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Microdeletion syndromes

Časopis lékařů českých, 2002-06, Vol.141 (12), p.363

Seemanová, E

2002

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DNA analysis of chromosome Y in the area of the azoospermia factor (AZF) in infertile men

Ceská gynekologie, 2001-09, Vol.66 (5), p.329

2001

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Importance of genetic testing in couples with reproductive disorders

Ceská gynekologie, 2004-01, Vol.69 (1), p.66

2004

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The interphase fluorescence in situ hybridization (I-FISH) technique in patients with chronic lymphatic leukemia (CLL)

Časopis lékařů českých, 2000-06, Vol.139 (11), p.334

2000

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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

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

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

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

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

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

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

Mutagenic effect of advanced paternal age in neurocardiofaciocutaneous syndrome

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

Clinical relevance of chromosomal aberrations in bone and soft tissue tumors in children and young adults

Chromosome instability syndromes

Microdeletion of the azoospermia factor as one of the causes of male infertility

Molecular diagnosis of haemophilia A in clinical practice

Increased risk of malignancies in heterozygotes in families of patients with Nijmegen breakage syndrome

Mosaic phenotypes

Pericentric inversion of human chromosomes and its risks

Chromosome markers and balanced translocation in the etiology of infertility

Microdeletion syndromes

DNA analysis of chromosome Y in the area of the azoospermia factor (AZF) in infertile men

Importance of genetic testing in couples with reproductive disorders

The interphase fluorescence in situ hybridization (I-FISH) technique in patients with chronic lymphatic leukemia (CLL)

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