Publications by authors named "Petr Goetz"

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The bleeding risk during warfarin therapy is associated with the number of variant alleles of CYP2C9 and VKORC1 genes.
Aleš Tomek, Václav Maťoška, Tereza Kolářová, Jiří Neumann, Martin Srámek, Petr Goetz

Cardiology· March 2014

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[Commentary: preimplantation genetic diagnosis].
Petr Goetz

Klin Onkol· December 2009

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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.
Martina Putzova, Lubomira Pecnova, Lucie Dvorakova, Inna Soldatova, Petr Goetz

Prenat Diagn· December 2008

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[Informed consent in medical genetics].
Petr Goetz

Cas Lek Cesk· September 2008

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QF-PCR-based prenatal detection of common aneuploidies in the Czech population: five years of experience.
Martina Putzova, Inna Soldatova, Lubomira Pecnova, Lucie Dvorakova, Nada Jencikova, Petr Goetz

Eur J Med Genet· August 2008

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Polymorphisms and low plasma activity of dopamine-beta-hydroxylase in ADHD children.
Marta Kopecková, Ivo Paclt, Petr Goetz

Neuro Endocrinol Lett· December 2006

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Genotype/phenotype correlation in a SCA1 family: anticipation without CAG expansion.
Peter O Bauer, Vaclav Matoska, Alena Zumrova, Arpad Boday, Hiroshi Doi, Petr Goetz

J Appl Genet· October 2005

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Large de novo expansion of CAG repeats in patient with sporadic spinocerebellar ataxia type 7.
Peter Bauer, Josef Kraus, Vaclav Matoska, Martina Brouckova, Alena Zumrova, Petr Goetz

J Neurol· August 2004

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DiGeorge/velocardiofacial syndrome: FISH studies of chromosomes 22q11 and 10p14, and clinical reports on the proximal 22q11 deletion.
Oliver Bartsch, Michaela Nemecková, Eduard Kocárek, Annett Wagner, Alena Puchmajerová, Petr Goetz

Am J Med Genet A· February 2003

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Is there anticipation in the age at onset of cancer in families with Li-Fraumeni syndrome?
Marie Trkova, Marie Hladikova, Pavel Kasal, Petr Goetz, Zdenek Sedlacek

J Hum Genet· October 2002

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