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Peter Gustavsson

Showing results (1-10 of 33) with videos related to

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Upsala Journal of Medical Sciences|September 26, 2002
Merging classical and modern genetic tools in the identification of disease genesPeter Gustavsson
Birth Defects Research. Part A, Clinical and Molecular Teratology|August 8, 2008
Grainyhead genes and mammalian neural tube closurePeter Gustavsson, Andrew J Copp, Nicholas D E Greene
Journal of Genetic Counseling|August 3, 2016
Knowledge and Attitudes Regarding Non-Invasive Prenatal Testing (NIPT) and Preferences for Risk Information among High School Students in SwedenSusanne Georgsson, Ellika Sahlin, Moa Iwarsson, et al.
Plos One|May 20, 2016
Positive Attitudes towards Non-Invasive Prenatal Testing (NIPT) in a Swedish Cohort of 1,003 Pregnant WomenEllika Sahlin, Magnus Nordenskjöld, Peter Gustavsson, et al.
European Journal of Medical Genetics|March 28, 2007
Duplication 16q12.1-q22.1 characterized by array CGH in a girl with spina bifidaPeter Gustavsson, Jacqueline Schoumans, Johan Staaf, et al.
Cerebellum (London, England)|March 13, 2018
Novel Features and Abnormal Pattern of Cerebral Glucose Metabolism in Spinocerebellar Ataxia 19Martin Paucar, Åsa Bergendal, Peter Gustavsson, et al.
Fetal Diagnosis and Therapy|July 26, 2014
Molecular and cytogenetic analysis in stillbirth: results from 481 consecutive casesEllika Sahlin, Peter Gustavsson, Agne Liedén, et al.
Human Mutation|December 30, 2017
Targeted copy number screening highlights an intragenic deletion of WDR63 as the likely cause of human occipital encephalocele and abnormal CNS development in zebrafishWolfgang Hofmeister, Maria Pettersson, Deniz Kurtoglu, et al.
Human Genetics|April 6, 2002
Linkage analysis identifies the thyroglobulin gene region as a major locus for familial congenital hypothyroidismBodil Edman Ahlbom, Muhammad Yaqoob, Peter Gustavsson, et al.
Molecular Genetics & Genomic Medicine|December 15, 2019
Pathogenic copy number variants are detected in a subset of patients with gastrointestinal malformationsJohanna Winberg, Peter Gustavsson, Ellika Sahlin, et al.
Pageof 4

Showing results (1-10 of 33) with videos related to

Sort By:
Pageof 4
Upsala Journal of Medical Sciences|September 26, 2002
Merging classical and modern genetic tools in the identification of disease genesPeter Gustavsson
Birth Defects Research. Part A, Clinical and Molecular Teratology|August 8, 2008
Grainyhead genes and mammalian neural tube closurePeter Gustavsson, Andrew J Copp, Nicholas D E Greene
Journal of Genetic Counseling|August 3, 2016
Knowledge and Attitudes Regarding Non-Invasive Prenatal Testing (NIPT) and Preferences for Risk Information among High School Students in SwedenSusanne Georgsson, Ellika Sahlin, Moa Iwarsson, et al.
Plos One|May 20, 2016
Positive Attitudes towards Non-Invasive Prenatal Testing (NIPT) in a Swedish Cohort of 1,003 Pregnant WomenEllika Sahlin, Magnus Nordenskjöld, Peter Gustavsson, et al.
European Journal of Medical Genetics|March 28, 2007
Duplication 16q12.1-q22.1 characterized by array CGH in a girl with spina bifidaPeter Gustavsson, Jacqueline Schoumans, Johan Staaf, et al.
Cerebellum (London, England)|March 13, 2018
Novel Features and Abnormal Pattern of Cerebral Glucose Metabolism in Spinocerebellar Ataxia 19Martin Paucar, Åsa Bergendal, Peter Gustavsson, et al.
Fetal Diagnosis and Therapy|July 26, 2014
Molecular and cytogenetic analysis in stillbirth: results from 481 consecutive casesEllika Sahlin, Peter Gustavsson, Agne Liedén, et al.
Human Mutation|December 30, 2017
Targeted copy number screening highlights an intragenic deletion of WDR63 as the likely cause of human occipital encephalocele and abnormal CNS development in zebrafishWolfgang Hofmeister, Maria Pettersson, Deniz Kurtoglu, et al.
Human Genetics|April 6, 2002
Linkage analysis identifies the thyroglobulin gene region as a major locus for familial congenital hypothyroidismBodil Edman Ahlbom, Muhammad Yaqoob, Peter Gustavsson, et al.
Molecular Genetics & Genomic Medicine|December 15, 2019
Pathogenic copy number variants are detected in a subset of patients with gastrointestinal malformationsJohanna Winberg, Peter Gustavsson, Ellika Sahlin, et al.
Pageof 4