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Methylation changes in promoter and enhancer regions of the WT1 gene in Wilms’ tumours

Cancer letters, 2001-05, Vol.166 (2), p.165-171

2001

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Mechanism and Genotype-Phenotype Correlation of Two Proximal 6q Deletions Characterized Using mBAND, FISH, Array CGH, and DNA Sequencing

Cytogenetic and genome research, 2012-01, Vol.136 (1), p.15-20

2012

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The human genome and medicine

Časopis lékařů českých, 2002, Vol.141 (1), p.8

Sedlácek, Z

2002

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Linear Vlasov plasma oscillations in the Fourier transformed velocity space

Physics letters. A, 2002-04, Vol.296 (2), p.117-124

2002

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Sternobronchial fistula--uncommon complication after coronary surgery (a case report)

Acta medica Lékarskí fakulty Univerzity Karlovy v Hradci Králove, 2000, Vol.43 (1), p.29-31

2000

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Is there anticipation in the age at onset of cancer in families with Li-Fraumeni syndrome?

Journal of human genetics, 2002-08, Vol.47 (8), p.381-386

2002

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Oncogene amplification and expression in pediatric solid tumors

Neoplasma, 1998, Vol.45 (3), p.123

1998

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When is it useful to look for TP53 germline gene mutations in families of oncology patients?

Časopis lékařů českých, 2003, Vol.142 (4), p.220

2003

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Two Li-Fraumeni syndrome families with novel germline p53 mutations : loss of the wild-type p53 allele in only 50% of tumours

British journal of cancer, 1998-04, Vol.77 (7), p.1034-1039

1998

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The human genome--chromosome X. Focus on Xq28

Časopis lékařů českých, 1995-12, Vol.134 (23), p.760

Sedlácek, Z

1995

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1419 POSTER Adrenal cortical tumours in childhood and adolescence, single institution experience

European journal of cancer supplements, 2007, Vol.5 (4), p.183-183

2007

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Expanded DMPK repeats in dizygotic twins referred for diagnosis of autism versus absence of expanded DMPK repeats at screening of 330 children with autism

Neuropsychiatric disease and treatment, 2016-01, Vol.12, p.2367-2372

2016

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Identification of five new families strengthens the link between childhood choroid plexus carcinoma and germline TP53 mutations

European journal of cancer (1990), 2005-07, Vol.41 (11), p.1597-1603

2005

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Genetics of autism

Časopis lékařů českých, 2002-06, Vol.141 (12), p.376

2002

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Molecular cloning and analysis of breakpoints on ring chromosome 17 in a patient with autism

Gene, 2008-01, Vol.407 (1), p.186-192

2008

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Stationary equilibria of a collisionless plasma treated by the moment method

Plasma physics, 1967-01, Vol.9 (3), p.255-274

Sedlácek, Z

1967

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A novel insertion of a rearranged L1 element in exon 44 of the dystrophin gene: Further evidence for possible bias in retroposon integration

Biochemical and biophysical research communications, 2006-08, Vol.347 (1), p.145-149

2006

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SECURITY QUESTIONS OF THE USE OF SMART MOBILE PHONES BY ELEMENTARY SCHOOL STUDENTS

Trends in Education, 2023-01, Vol.15 (1)

2023

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Torsion of the spleen--an unusual cause of sudden acute abdomen

Rozhledy v chirurgii, 2002-09, Vol.81 (9), p.492

2002

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DNA methylation and neoplasms

Časopis lékařů českých, 2000-05, Vol.139 (10), p.291

2000

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Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders

EUROPEAN JOURNAL OF HUMAN GENETICS, 2020, Vol.28 (SUPPL 1), p.3

2020

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Diagnosis of spontaneous arteriovenous fistula complicating aortoiliac aneurysm using spiral CT. Report of 3 cases

Rozhledy v chirurgii, 2004-10, Vol.83 (10), p.493

2004

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Detailed analysis of chromosome rearrangements in patients with autism and mental retardation

New biotechnology, 2010-04, Vol.27, p.S65-S65

2010

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Neolitická osada v Ohrade u Kolína

Archeologické rozhledy (Praha), 1994-01, Vol.46 (3), p.410-428

1994

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Methylation changes in promoter and enhancer regions of the WT1 gene in Wilms’ tumours

Mechanism and Genotype-Phenotype Correlation of Two Proximal 6q Deletions Characterized Using mBAND, FISH, Array CGH, and DNA Sequencing

Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domains

The human genome and medicine

Linear Vlasov plasma oscillations in the Fourier transformed velocity space

Sternobronchial fistula--uncommon complication after coronary surgery (a case report)

Is there anticipation in the age at onset of cancer in families with Li-Fraumeni syndrome?

Oncogene amplification and expression in pediatric solid tumors

When is it useful to look for TP53 germline gene mutations in families of oncology patients?

Two Li-Fraumeni syndrome families with novel germline p53 mutations : loss of the wild-type p53 allele in only 50% of tumours

The human genome--chromosome X. Focus on Xq28

1419 POSTER Adrenal cortical tumours in childhood and adolescence, single institution experience

Expanded DMPK repeats in dizygotic twins referred for diagnosis of autism versus absence of expanded DMPK repeats at screening of 330 children with autism

Identification of five new families strengthens the link between childhood choroid plexus carcinoma and germline TP53 mutations

Genetics of autism

Molecular cloning and analysis of breakpoints on ring chromosome 17 in a patient with autism

Stationary equilibria of a collisionless plasma treated by the moment method

A novel insertion of a rearranged L1 element in exon 44 of the dystrophin gene: Further evidence for possible bias in retroposon integration

SECURITY QUESTIONS OF THE USE OF SMART MOBILE PHONES BY ELEMENTARY SCHOOL STUDENTS

Torsion of the spleen--an unusual cause of sudden acute abdomen

DNA methylation and neoplasms

Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders

Diagnosis of spontaneous arteriovenous fistula complicating aortoiliac aneurysm using spiral CT. Report of 3 cases

Detailed analysis of chromosome rearrangements in patients with autism and mental retardation

Neolitická osada v Ohrade u Kolína

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