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A rare cause of mediastinal expansion with a massive pleural effusion

Postgraduate medical journal, 2005-11, Vol.81 (961), p.e18-e18

2005

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HCFC1 loss-of-function mutations disrupt neuronal and neural progenitor cells of the developing brain

Human molecular genetics, 2015-06, Vol.24 (12), p.3335-3347

2015

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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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The expression of PAX5, p53 immunohistochemistry and p53 mutation analysis in superficial bladder carcinoma tissue. Correlation with pathological findings and clinical outcome

International urology and nephrology, 2002, Vol.34 (4), p.495-501

2002

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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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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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A database of germline p53 mutations in cancer-prone families

Nucleic acids research, 1998-01, Vol.26 (1), p.214

1998

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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 amphioxus rab GDP-dissociation inhibitor (GDI) gene is neural-specific: implications for the evolution of chordate rab GDI genes

Molecular biology and evolution, 1999-09, Vol.16 (9), p.1231-1237

1999

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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

Volltextzugriff (PDF)

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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Not EEG abnormalities but epilepsy is associated with autistic regression and mental functioning in childhood autism

European child & adolescent psychiatry, 2004-08, Vol.13 (4), p.209-213

2004

Volltextzugriff (PDF)

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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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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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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A Complex Pattern of Evolutionary Conservation and Alternative Polyadenylation Within the Long 3′-Untranslated Region of the Methyl-CpG-Binding Protein 2 Gene (MeCP2) Suggests a Regulatory Role in Gene Expression

Human molecular genetics, 1999-07, Vol.8 (7), p.1253-1262

1999

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Subtypes of autism by cluster analysis based on structural MRI data

European child & adolescent psychiatry, 2005-06, Vol.14 (3), p.138-144

2005

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A rare cause of mediastinal expansion with a massive pleural effusion

HCFC1 loss-of-function mutations disrupt neuronal and neural progenitor cells of the developing brain

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

The expression of PAX5, p53 immunohistochemistry and p53 mutation analysis in superficial bladder carcinoma tissue. Correlation with pathological findings and clinical outcome

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

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?

A database of germline p53 mutations in cancer-prone families

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 amphioxus rab GDP-dissociation inhibitor (GDI) gene is neural-specific: implications for the evolution of chordate rab GDI genes

The human genome--chromosome X. Focus on Xq28

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

Not EEG abnormalities but epilepsy is associated with autistic regression and mental functioning in childhood autism

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

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

DNA methylation and neoplasms

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

A Complex Pattern of Evolutionary Conservation and Alternative Polyadenylation Within the Long 3′-Untranslated Region of the Methyl-CpG-Binding Protein 2 Gene (MeCP2) Suggests a Regulatory Role in Gene Expression

Subtypes of autism by cluster analysis based on structural MRI data

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