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Franco Laccone

Showing results (1-10 of 99) with videos related to

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Methods in Molecular Biology (Clifton, N.J.)|December 24, 2002
A fast polymerase chain reaction-mediated strategy for introducing repeat expansions into CAG-repeat containing genesFranco Laccone
International Journal of Molecular Medicine|October 4, 2006
Williams-Beuren syndrome: determination of deletion size using quantitative real-time PCRCornelia Schubert, Franco Laccone
The American Journal of Case Reports|November 25, 2020
Phenotypic Heterogeneity in 5 Family Members with the Mitochondrial Variant m.3243A>GJosef Finsterer, Franco Laccone
Metabolic Brain Disease|June 2, 2019
Autosomal dominant optic atrophy plus due to the novel OPA1 variant c.1463G>CJosef Finsterer, Franco Laccone
Human Mutation|July 23, 2003
Mutations and polymorphisms in the human methyl CpG-binding protein MECP2Gabriel Miltenberger-Miltenyi, Franco Laccone
Acta Cardiologica|July 26, 2021
Noncompaction and the novel variant c.425A>T in <i>TPM1</i>Josef Finsterer, Claudia Stöllberger, Franco Laccone
Annals of Indian Academy of Neurology|March 17, 2017
Pregnancy reduces severity and frequency of attacks in hyperkalemic periodic paralysis due to the mutation c.2111C>T in the <i>SCN4A</i> geneJosef Finsterer, Salma Majid Wakil, Franco Laccone
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|April 10, 2019
Familial, long-term pollakisuria as initial manifestation of HSP4 due to the SPAST variant c.683-2A>CJosef Finsterer, Salma M Wakil, Franco Laccone
The Journal of Pediatrics|March 18, 2003
Indication for genetic testing: a checklist for Rett syndromePeter Huppke, Karola Köhler, Franco Laccone, et al.
Journal of Neurosciences in Rural Practice|May 6, 2020
Variants in <i>HNRNPDL</i> and <i>SETX</i> Not Necessarily Indicate Familial Amyotrophic Lateral Sclerosis or Limb Girdle Muscular Dystrophy 1G in Acute Muscular Respiratory FailureJosef Finsterer, Claudia Stöllberger, Hans Keller, et al.
Pageof 10

Showing results (1-10 of 99) with videos related to

Sort By:
Pageof 10
Methods in Molecular Biology (Clifton, N.J.)|December 24, 2002
A fast polymerase chain reaction-mediated strategy for introducing repeat expansions into CAG-repeat containing genesFranco Laccone
International Journal of Molecular Medicine|October 4, 2006
Williams-Beuren syndrome: determination of deletion size using quantitative real-time PCRCornelia Schubert, Franco Laccone
The American Journal of Case Reports|November 25, 2020
Phenotypic Heterogeneity in 5 Family Members with the Mitochondrial Variant m.3243A>GJosef Finsterer, Franco Laccone
Metabolic Brain Disease|June 2, 2019
Autosomal dominant optic atrophy plus due to the novel OPA1 variant c.1463G>CJosef Finsterer, Franco Laccone
Human Mutation|July 23, 2003
Mutations and polymorphisms in the human methyl CpG-binding protein MECP2Gabriel Miltenberger-Miltenyi, Franco Laccone
Acta Cardiologica|July 26, 2021
Noncompaction and the novel variant c.425A>T in <i>TPM1</i>Josef Finsterer, Claudia Stöllberger, Franco Laccone
Annals of Indian Academy of Neurology|March 17, 2017
Pregnancy reduces severity and frequency of attacks in hyperkalemic periodic paralysis due to the mutation c.2111C>T in the <i>SCN4A</i> geneJosef Finsterer, Salma Majid Wakil, Franco Laccone
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|April 10, 2019
Familial, long-term pollakisuria as initial manifestation of HSP4 due to the SPAST variant c.683-2A>CJosef Finsterer, Salma M Wakil, Franco Laccone
The Journal of Pediatrics|March 18, 2003
Indication for genetic testing: a checklist for Rett syndromePeter Huppke, Karola Köhler, Franco Laccone, et al.
Journal of Neurosciences in Rural Practice|May 6, 2020
Variants in <i>HNRNPDL</i> and <i>SETX</i> Not Necessarily Indicate Familial Amyotrophic Lateral Sclerosis or Limb Girdle Muscular Dystrophy 1G in Acute Muscular Respiratory FailureJosef Finsterer, Claudia Stöllberger, Hans Keller, et al.
Pageof 10