P. Goetz

发表

Absence of spinocerebellar ataxia type 3/Machado–Joseph disease within ataxic patients in the Czech population

V. Maťoška, T. Maříková, P. O. Bauer, 2005, European journal of neurology.

Polymorphisms of dopamine-beta-hydroxylase in ADHD children.

I. Paclt, P. Goetz, M. Kopečková, 2006, Folia biologica.

Polymorphisms of Dopamine-β-Hydroxylase in ADHD Children ( dopamine-β-hydroxylase / plasma activity / ADHD / polymorphism / G 444 A / G

I. Paclt, P. Goetz, M. Kopečková, 2022 .

Fluorescent Multiplex PCR: Fast Method for Autosomal Dominant Spinocerebellar Ataxias Screening

N. Nukina, P. Hedvičáková, A. Tomek, 2005, Russian Journal of Genetics.

Genotype/phenotype correlation in a SCA1 family: anticipation without CAG expansion.

H. Doi, P. Bauer, V. Maťoška, 2005, Journal of applied genetics.

Polymorphisms and low plasma activity of dopamine-beta-hydroxylase in ADHD children.

I. Paclt, P. Goetz, M. Kopečková, 2006, Neuro endocrinology letters.

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

M. Trková, Z. Sedlacek, P. Goetz, 2002, Journal of Human Genetics.

OmniPlex—a new QF‐PCR assay for prenatal diagnosis of common aneuploidies based on evaluation of the heterozygosity of short tandem repeat loci in the Czech population

L. Dvorakova, D. Stejskal, P. Goetz, 2008, Prenatal diagnosis.

Can ataxin-2 be down-regulated by allele-specific de novo DNA methylation in SCA2 patients?

P. Bauer, V. Maťoška, A. Zumrová, 2004, Medical hypotheses.

Clinical findings with implications for genetic testing in families with clustering of colorectal cancer.

A. Zwinderman, K. Heimdal, P. Møller, 1998, The New England journal of medicine.

The Bleeding Risk during Warfarin Therapy Is Associated with the Number of Variant Alleles of CYP2C9 and VKORC1 Genes

V. Serebruany, M. Bojar, A. Tomek, 2013, Cardiology.

QF-PCR-based prenatal detection of common aneuploidies in the Czech population: five years of experience.

L. Dvorakova, D. Stejskal, P. Goetz, 2008, European journal of medical genetics.

Large de novo expansion of CAG repeats in patient with sporadic spinocerebellar ataxia type 7

P. Bauer, V. Maťoška, J. Kraus, 2004, Journal of Neurology.