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Peter Gustavsson

Showing results (21-30 of 33) with videos related to

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Journal of the Neurological Sciences|April 20, 2024
Novel findings in a Swedish primary familial brain calcification cohortStefan Sennfält, Peter Gustavsson, Helena Malmgren, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 9, 2011
Copy number variation characteristics in subpopulations of patients with autism spectrum disordersAnna Bremer, MaiBritt Giacobini, Mats Eriksson, et al.
American Journal of Medical Genetics. Part A|August 31, 2010
Chimerism resulting from parthenogenetic activation and dispermic fertilizationJohanna Winberg, Peter Gustavsson, Kristina Lagerstedt-Robinson, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|June 5, 2013
Is LMNB1 a susceptibility gene for neural tube defects in humans?Alexis Robinson, Darren Partridge, Ashraf Malhas, et al.
Human Molecular Genetics|September 7, 2018
Overexpression of Grainyhead-like 3 causes spina bifida and interacts genetically with mutant alleles of Grhl2 and Vangl2 in miceSandra C P De Castro, Peter Gustavsson, Abigail R Marshall, et al.
Human Mutation|November 19, 2016
Whole-Genome Sequencing of Cytogenetically Balanced Chromosome Translocations Identifies Potentially Pathological Gene Disruptions and Highlights the Importance of Microhomology in the Mechanism of FormationDaniel Nilsson, Maria Pettersson, Peter Gustavsson, et al.
Human Molecular Genetics|October 20, 2007
Alpha-cardiac actin mutations produce atrial septal defectsHans Matsson, Jacqueline Eason, Carol S Bookwalter, et al.
Journal of Medical Genetics|November 9, 2013
Different mutations in PDE4D associated with developmental disorders with mirror phenotypesAnna Lindstrand, Giedre Grigelioniene, Daniel Nilsson, et al.
Human Molecular Genetics|December 16, 2011
Mutations in genes encoding the glycine cleavage system predispose to neural tube defects in mice and humansAyumi Narisawa, Shoko Komatsuzaki, Atsuo Kikuchi, et al.
Scientific Reports|June 25, 2016
De novo intrachromosomal gene conversion from OPN1MW to OPN1LW in the male germline results in Blue Cone MonochromacyElena Buena-Atienza, Klaus Rüther, Britta Baumann, et al.
Pageof 4

Showing results (21-30 of 33) with videos related to

Sort By:
Pageof 4
Journal of the Neurological Sciences|April 20, 2024
Novel findings in a Swedish primary familial brain calcification cohortStefan Sennfält, Peter Gustavsson, Helena Malmgren, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 9, 2011
Copy number variation characteristics in subpopulations of patients with autism spectrum disordersAnna Bremer, MaiBritt Giacobini, Mats Eriksson, et al.
American Journal of Medical Genetics. Part A|August 31, 2010
Chimerism resulting from parthenogenetic activation and dispermic fertilizationJohanna Winberg, Peter Gustavsson, Kristina Lagerstedt-Robinson, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|June 5, 2013
Is LMNB1 a susceptibility gene for neural tube defects in humans?Alexis Robinson, Darren Partridge, Ashraf Malhas, et al.
Human Molecular Genetics|September 7, 2018
Overexpression of Grainyhead-like 3 causes spina bifida and interacts genetically with mutant alleles of Grhl2 and Vangl2 in miceSandra C P De Castro, Peter Gustavsson, Abigail R Marshall, et al.
Human Mutation|November 19, 2016
Whole-Genome Sequencing of Cytogenetically Balanced Chromosome Translocations Identifies Potentially Pathological Gene Disruptions and Highlights the Importance of Microhomology in the Mechanism of FormationDaniel Nilsson, Maria Pettersson, Peter Gustavsson, et al.
Human Molecular Genetics|October 20, 2007
Alpha-cardiac actin mutations produce atrial septal defectsHans Matsson, Jacqueline Eason, Carol S Bookwalter, et al.
Journal of Medical Genetics|November 9, 2013
Different mutations in PDE4D associated with developmental disorders with mirror phenotypesAnna Lindstrand, Giedre Grigelioniene, Daniel Nilsson, et al.
Human Molecular Genetics|December 16, 2011
Mutations in genes encoding the glycine cleavage system predispose to neural tube defects in mice and humansAyumi Narisawa, Shoko Komatsuzaki, Atsuo Kikuchi, et al.
Scientific Reports|June 25, 2016
De novo intrachromosomal gene conversion from OPN1MW to OPN1LW in the male germline results in Blue Cone MonochromacyElena Buena-Atienza, Klaus Rüther, Britta Baumann, et al.
Pageof 4