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Moyra Smith

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

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BMC Medical Genetics|April 20, 2004
A case of autism with an interstitial deletion on 4q leading to hemizygosity for genes encoding for glutamine and glycine neurotransmitter receptor sub-units (AMPA 2, GLRA3, GLRB) and neuropeptide receptors NPY1R, NPY5RSubhadra Ramanathan, Abigail Woodroffe, Pamela L Flodman, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 14, 2005
Evaluation of the chromosome 2q37.3 gene CENTG2 as an autism susceptibility geneThomas H Wassink, Joseph Piven, Veronica J Vieland, et al.
Biochimica Et Biophysica Acta|April 28, 2012
Mitochondrial and ion channel gene alterations in autismMoyra Smith, Pamela L Flodman, John J Gargus, et al.
Annals of Neurology|June 5, 2003
Mitochondrial dysfunction in autistic patients with 15q inverted duplicationPauline A Filipek, Jenifer Juranek, Moyra Smith, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 30, 2004
Alleles of a reelin CGG repeat do not convey liability to autism in a sample from the CPEA networkBernie Devlin, Pamela Bennett, Geraldine Dawson, et al.
American Journal of Human Genetics|June 12, 2002
Presence of large deletions in kindreds with autismChang-En Yu, Geraldine Dawson, Jeffrey Munson, et al.
Iscience|July 19, 2024
Circulating biomarkers of kidney angiomyolipoma and cysts in tuberous sclerosis complex patientsVarvara I Rubtsova, Yujin Chun, Joohwan Kim, et al.
Journal of Medical Genetics|June 11, 2020
<i>NUBPL</i> mitochondrial disease: new patients and review of the genetic and clinical spectrumVirginia Kimonis, Rehab Al Dubaisi, Andrew E Maclean, et al.
Nature Genetics|August 18, 2022
Rare coding variation provides insight into the genetic architecture and phenotypic context of autismJack M Fu, F Kyle Satterstrom, Minshi Peng, et al.
Nature Genetics|February 27, 2007
Mapping autism risk loci using genetic linkage and chromosomal rearrangements, Peter Szatmari, Andrew D Paterson, et al.
Pageof 2

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

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
BMC Medical Genetics|April 20, 2004
A case of autism with an interstitial deletion on 4q leading to hemizygosity for genes encoding for glutamine and glycine neurotransmitter receptor sub-units (AMPA 2, GLRA3, GLRB) and neuropeptide receptors NPY1R, NPY5RSubhadra Ramanathan, Abigail Woodroffe, Pamela L Flodman, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 14, 2005
Evaluation of the chromosome 2q37.3 gene CENTG2 as an autism susceptibility geneThomas H Wassink, Joseph Piven, Veronica J Vieland, et al.
Biochimica Et Biophysica Acta|April 28, 2012
Mitochondrial and ion channel gene alterations in autismMoyra Smith, Pamela L Flodman, John J Gargus, et al.
Annals of Neurology|June 5, 2003
Mitochondrial dysfunction in autistic patients with 15q inverted duplicationPauline A Filipek, Jenifer Juranek, Moyra Smith, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 30, 2004
Alleles of a reelin CGG repeat do not convey liability to autism in a sample from the CPEA networkBernie Devlin, Pamela Bennett, Geraldine Dawson, et al.
American Journal of Human Genetics|June 12, 2002
Presence of large deletions in kindreds with autismChang-En Yu, Geraldine Dawson, Jeffrey Munson, et al.
Iscience|July 19, 2024
Circulating biomarkers of kidney angiomyolipoma and cysts in tuberous sclerosis complex patientsVarvara I Rubtsova, Yujin Chun, Joohwan Kim, et al.
Journal of Medical Genetics|June 11, 2020
<i>NUBPL</i> mitochondrial disease: new patients and review of the genetic and clinical spectrumVirginia Kimonis, Rehab Al Dubaisi, Andrew E Maclean, et al.
Nature Genetics|August 18, 2022
Rare coding variation provides insight into the genetic architecture and phenotypic context of autismJack M Fu, F Kyle Satterstrom, Minshi Peng, et al.
Nature Genetics|February 27, 2007
Mapping autism risk loci using genetic linkage and chromosomal rearrangements, Peter Szatmari, Andrew D Paterson, et al.
Pageof 2