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Gudrun Nygren

Showing results (21-30 of 38) with videos related to

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BMC Medical Genetics|July 7, 2010
Mutation screening of NOS1AP gene in a large sample of psychiatric patients and controlsRichard Delorme, Catalina Betancur, Isabelle Scheid, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 12, 2007
Mutation screening of the PTEN gene in patients with autism spectrum disorders and macrocephalyJoseph D Buxbaum, Guiqing Cai, Pauline Chaste, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 7, 2005
Expression and genetic variability of PCDH11Y, a gene specific to Homo sapiens and candidate for susceptibility to psychiatric disordersChristelle M Durand, Caroline Kappeler, Catalina Betancur, et al.
BMC Medical Genetics|January 27, 2009
An investigation of ribosomal protein L10 gene in autism spectrum disordersXiaohong Gong, Richard Delorme, Fabien Fauchereau, et al.
Plos One|March 12, 2011
Variations of the candidate SEZ6L2 gene on Chromosome 16p11.2 in patients with autism spectrum disorders and in human populationsMarina Konyukh, Richard Delorme, Pauline Chaste, et al.
Biological Psychiatry|April 4, 2006
No human tryptophan hydroxylase-2 gene R441H mutation in a large cohort of psychiatric patients and control subjectsRichard Delorme, Christelle M Durand, Catalina Betancur, et al.
BMC Medical Genetics|December 5, 2013
Heterozygous FA2H mutations in autism spectrum disordersIsabelle Scheid, Anna Maruani, Guillaume Huguet, et al.
Molecular Autism|April 7, 2015
Complex nature of apparently balanced chromosomal rearrangements in patients with autism spectrum disorderAnne-Claude Tabet, Alain Verloes, Marion Pilorge, et al.
Plos One|July 27, 2010
Identification of pathway-biased and deleterious melatonin receptor mutants in autism spectrum disorders and in the general populationPauline Chaste, Nathalie Clement, Oriane Mercati, et al.
Biological Psychiatry|March 13, 2009
Screening for genomic rearrangements and methylation abnormalities of the 15q11-q13 region in autism spectrum disordersChristel Depienne, Daniel Moreno-De-Luca, Delphine Heron, et al.
Pageof 4

Showing results (21-30 of 38) with videos related to

Sort By:
Pageof 4
BMC Medical Genetics|July 7, 2010
Mutation screening of NOS1AP gene in a large sample of psychiatric patients and controlsRichard Delorme, Catalina Betancur, Isabelle Scheid, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 12, 2007
Mutation screening of the PTEN gene in patients with autism spectrum disorders and macrocephalyJoseph D Buxbaum, Guiqing Cai, Pauline Chaste, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 7, 2005
Expression and genetic variability of PCDH11Y, a gene specific to Homo sapiens and candidate for susceptibility to psychiatric disordersChristelle M Durand, Caroline Kappeler, Catalina Betancur, et al.
BMC Medical Genetics|January 27, 2009
An investigation of ribosomal protein L10 gene in autism spectrum disordersXiaohong Gong, Richard Delorme, Fabien Fauchereau, et al.
Plos One|March 12, 2011
Variations of the candidate SEZ6L2 gene on Chromosome 16p11.2 in patients with autism spectrum disorders and in human populationsMarina Konyukh, Richard Delorme, Pauline Chaste, et al.
Biological Psychiatry|April 4, 2006
No human tryptophan hydroxylase-2 gene R441H mutation in a large cohort of psychiatric patients and control subjectsRichard Delorme, Christelle M Durand, Catalina Betancur, et al.
BMC Medical Genetics|December 5, 2013
Heterozygous FA2H mutations in autism spectrum disordersIsabelle Scheid, Anna Maruani, Guillaume Huguet, et al.
Molecular Autism|April 7, 2015
Complex nature of apparently balanced chromosomal rearrangements in patients with autism spectrum disorderAnne-Claude Tabet, Alain Verloes, Marion Pilorge, et al.
Plos One|July 27, 2010
Identification of pathway-biased and deleterious melatonin receptor mutants in autism spectrum disorders and in the general populationPauline Chaste, Nathalie Clement, Oriane Mercati, et al.
Biological Psychiatry|March 13, 2009
Screening for genomic rearrangements and methylation abnormalities of the 15q11-q13 region in autism spectrum disordersChristel Depienne, Daniel Moreno-De-Luca, Delphine Heron, et al.
Pageof 4