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Henriett Pikó

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Ideggyogyaszati Szemle|December 17, 2008
[Screening for hereditary neuromuscular disorders with molecular genetic methods in the Roma population of Hungary]Agnes Herczegfalvi, Henriett Pikó, Veronika Karcagi
Avian Pathology : Journal of the W.V.P.A|July 21, 2006
Class 1 integrons and their conjugal transfer with and without virulence-associated genes in extra-intestinal and intestinal Escherichia coli of poultryNoémi Nógrády, Judit Pászti, Henriett Pikó, et al.
Orvosi Hetilap|September 17, 2011
[Role of associated alleles and hypomethylation status in the clinical expression of facioscapulohumeral muscular dystrophy]Henriett Pikó, Mária Judit Molnár, Agnes Herczegfalvi, et al.
Orvosi Hetilap|December 7, 2007
[Carrier detection in families affected by Duchenne/Becker muscular dystrophy]Henriett Pikó, Bálint Nagy, Judit Balog, et al.
Neuromuscular Disorders : NMD|December 17, 2008
Dystrophin gene analysis in Hungarian Duchenne/Becker muscular dystrophy families - detection of carrier status in symptomatic and asymptomatic female relativesHenriett Pikó, Viktor Vancsó, Bálint Nagy, et al.
Molecular Cytogenetics|June 25, 2014
A de novo atypical ring sSMC(22) characterized by array CGH in a boy with cat-eye syndromeIrén Haltrich, Henriett Pikó, Eszter Kiss, et al.
Orvosi Hetilap|March 20, 2022
Genotype-phenotype correlation in a newborn with de novo 3p25 deletion syndromeEdina Sarkadi, Erika P Tardy, Henriett Pikó, et al.
BMC Medical Genomics|April 22, 2024
Screening of premature ovarian insufficiency associated genes in Hungarian patients with next generation sequencingAnett Illés, Henriett Pikó, Kristóf Árvai, et al.
Molecular Cytogenetics|November 2, 2022
Clinical evaluation of rare copy number variations identified by chromosomal microarray in a Hungarian neurodevelopmental disorder patient cohortAnna Lengyel, Éva Pinti, Henriett Pikó, et al.
Ideggyogyaszati Szemle|May 12, 2005
[Calpain-3 gene defect causing limb gird muscular dystrophy in a Hungarian family]Rita Horváth, Maggie C Walter, Hanns Lochmüller, et al.
Pageof 3

Showing results (1-10 of 25) with videos related to

Sort By:
Pageof 3
Ideggyogyaszati Szemle|December 17, 2008
[Screening for hereditary neuromuscular disorders with molecular genetic methods in the Roma population of Hungary]Agnes Herczegfalvi, Henriett Pikó, Veronika Karcagi
Avian Pathology : Journal of the W.V.P.A|July 21, 2006
Class 1 integrons and their conjugal transfer with and without virulence-associated genes in extra-intestinal and intestinal Escherichia coli of poultryNoémi Nógrády, Judit Pászti, Henriett Pikó, et al.
Orvosi Hetilap|September 17, 2011
[Role of associated alleles and hypomethylation status in the clinical expression of facioscapulohumeral muscular dystrophy]Henriett Pikó, Mária Judit Molnár, Agnes Herczegfalvi, et al.
Orvosi Hetilap|December 7, 2007
[Carrier detection in families affected by Duchenne/Becker muscular dystrophy]Henriett Pikó, Bálint Nagy, Judit Balog, et al.
Neuromuscular Disorders : NMD|December 17, 2008
Dystrophin gene analysis in Hungarian Duchenne/Becker muscular dystrophy families - detection of carrier status in symptomatic and asymptomatic female relativesHenriett Pikó, Viktor Vancsó, Bálint Nagy, et al.
Molecular Cytogenetics|June 25, 2014
A de novo atypical ring sSMC(22) characterized by array CGH in a boy with cat-eye syndromeIrén Haltrich, Henriett Pikó, Eszter Kiss, et al.
Orvosi Hetilap|March 20, 2022
Genotype-phenotype correlation in a newborn with de novo 3p25 deletion syndromeEdina Sarkadi, Erika P Tardy, Henriett Pikó, et al.
BMC Medical Genomics|April 22, 2024
Screening of premature ovarian insufficiency associated genes in Hungarian patients with next generation sequencingAnett Illés, Henriett Pikó, Kristóf Árvai, et al.
Molecular Cytogenetics|November 2, 2022
Clinical evaluation of rare copy number variations identified by chromosomal microarray in a Hungarian neurodevelopmental disorder patient cohortAnna Lengyel, Éva Pinti, Henriett Pikó, et al.
Ideggyogyaszati Szemle|May 12, 2005
[Calpain-3 gene defect causing limb gird muscular dystrophy in a Hungarian family]Rita Horváth, Maggie C Walter, Hanns Lochmüller, et al.
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