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Jozef Gecz

Showing results (11-20 of 244) with videos related to

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American Journal of Obstetrics and Gynecology|May 25, 2015
Cerebral palsy: causes, pathways, and the role of genetic variantsAlastair H MacLennan, Suzanna C Thompson, Jozef Gecz
American Journal of Medical Genetics. Part A|September 12, 2012
A novel contiguous gene deletion of AVPR2 and ARHGAP4 genes in male dizygotic twins with nephrogenic diabetes insipidus and intellectual disabilityLingli Huang, Gemma Poke, Jozef Gecz, et al.
Neuroscience and Biobehavioral Reviews|November 19, 2013
Nonsense-mediated mRNA decay: inter-individual variability and human diseaseLam Son Nguyen, Miles F Wilkinson, Jozef Gecz
American Journal of Obstetrics and Gynecology|February 2, 2016
ReplyAlastair Harvey Maclennan, Suzanna C Thompson, Jozef Gecz
Nature Reviews. Neurology|August 3, 2023
Redefining cerebral palsies as a diverse group of neurodevelopmental disorders with genetic aetiologyClare L van Eyk, Michael C Fahey, Jozef Gecz
European Journal of Human Genetics : EJHG|January 17, 2008
XLMR genes: update 2007Pietro Chiurazzi, Charles E Schwartz, Jozef Gecz, et al.
Cellular and Molecular Life Sciences : CMLS|February 13, 2015
La FAM fatale: USP9X in development and diseaseMariyam Murtaza, Lachlan A Jolly, Jozef Gecz, et al.
American Journal of Medical Genetics|October 12, 2002
Variable expression of mental retardation, autism, seizures, and dystonic hand movements in two families with an identical ARX gene mutationGillian Turner, Michael Partington, Bronwyn Kerr, et al.
Human Molecular Genetics|March 20, 2009
Lessons learnt from large-scale exon re-sequencing of the X chromosomeF Lucy Raymond, Annabel Whibley, Michael R Stratton, et al.
Human Molecular Genetics|October 15, 2013
Reduced polyalanine-expanded Arx mutant protein in developing mouse subpallium alters Lmo1 transcriptional regulationKristie Lee, Tessa Mattiske, Kunio Kitamura, et al.
Pageof 25

Showing results (11-20 of 244) with videos related to

Sort By:
Pageof 25
American Journal of Obstetrics and Gynecology|May 25, 2015
Cerebral palsy: causes, pathways, and the role of genetic variantsAlastair H MacLennan, Suzanna C Thompson, Jozef Gecz
American Journal of Medical Genetics. Part A|September 12, 2012
A novel contiguous gene deletion of AVPR2 and ARHGAP4 genes in male dizygotic twins with nephrogenic diabetes insipidus and intellectual disabilityLingli Huang, Gemma Poke, Jozef Gecz, et al.
Neuroscience and Biobehavioral Reviews|November 19, 2013
Nonsense-mediated mRNA decay: inter-individual variability and human diseaseLam Son Nguyen, Miles F Wilkinson, Jozef Gecz
American Journal of Obstetrics and Gynecology|February 2, 2016
ReplyAlastair Harvey Maclennan, Suzanna C Thompson, Jozef Gecz
Nature Reviews. Neurology|August 3, 2023
Redefining cerebral palsies as a diverse group of neurodevelopmental disorders with genetic aetiologyClare L van Eyk, Michael C Fahey, Jozef Gecz
European Journal of Human Genetics : EJHG|January 17, 2008
XLMR genes: update 2007Pietro Chiurazzi, Charles E Schwartz, Jozef Gecz, et al.
Cellular and Molecular Life Sciences : CMLS|February 13, 2015
La FAM fatale: USP9X in development and diseaseMariyam Murtaza, Lachlan A Jolly, Jozef Gecz, et al.
American Journal of Medical Genetics|October 12, 2002
Variable expression of mental retardation, autism, seizures, and dystonic hand movements in two families with an identical ARX gene mutationGillian Turner, Michael Partington, Bronwyn Kerr, et al.
Human Molecular Genetics|March 20, 2009
Lessons learnt from large-scale exon re-sequencing of the X chromosomeF Lucy Raymond, Annabel Whibley, Michael R Stratton, et al.
Human Molecular Genetics|October 15, 2013
Reduced polyalanine-expanded Arx mutant protein in developing mouse subpallium alters Lmo1 transcriptional regulationKristie Lee, Tessa Mattiske, Kunio Kitamura, et al.
Pageof 25