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Martin Poot

Showing results (91-100 of 100) with videos related to

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Cell Reports|July 21, 2012
Constitutional chromothripsis rearrangements involve clustered double-stranded DNA breaks and nonhomologous repair mechanismsWigard P Kloosterman, Masoumeh Tavakoli-Yaraki, Markus J van Roosmalen, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 24, 2009
A co-segregating microduplication of chromosome 15q11.2 pinpoints two risk genes for autism spectrum disorderBert van der Zwaag, Wouter G Staal, Ron Hochstenbach, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|June 10, 2011
No association between a common single nucleotide polymorphism, rs4141463, in the MACROD2 gene and autism spectrum disorderSarah Curran, Patrick Bolton, Kinga Rozsnyai, et al.
European Journal of Human Genetics : EJHG|November 28, 2013
Structural genomic variation in childhood epilepsies with complex phenotypesIngo Helbig, Marielle E M Swinkels, Emmelien Aten, et al.
Human Genetics|May 6, 2010
WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterationsKatrin Friedrich, Lin Lee, Dru F Leistritz, et al.
Human Mutation|September 27, 2016
WRN Mutation Update: Mutation Spectrum, Patient Registries, and Translational ProspectsKoutaro Yokote, Sirisak Chanprasert, Lin Lee, et al.
Plos One|June 4, 2009
Gene-network analysis identifies susceptibility genes related to glycobiology in autismBert van der Zwaag, Lude Franke, Martin Poot, et al.
Human Mutation|May 5, 2006
The spectrum of WRN mutations in Werner syndrome patientsShurong Huang, Lin Lee, Nancy B Hanson, et al.
Plos Genetics|February 21, 2012
Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disordersClaire S Leblond, Jutta Heinrich, Richard Delorme, et al.
The New England Journal of Medicine|September 12, 2008
Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypesHeather C Mefford, Andrew J Sharp, Carl Baker, et al.
Pageof 10

Showing results (91-100 of 100) with videos related to

Sort By:
Pageof 10
You have reached the last page of results.This site can display upto 100 results.
Cell Reports|July 21, 2012
Constitutional chromothripsis rearrangements involve clustered double-stranded DNA breaks and nonhomologous repair mechanismsWigard P Kloosterman, Masoumeh Tavakoli-Yaraki, Markus J van Roosmalen, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 24, 2009
A co-segregating microduplication of chromosome 15q11.2 pinpoints two risk genes for autism spectrum disorderBert van der Zwaag, Wouter G Staal, Ron Hochstenbach, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|June 10, 2011
No association between a common single nucleotide polymorphism, rs4141463, in the MACROD2 gene and autism spectrum disorderSarah Curran, Patrick Bolton, Kinga Rozsnyai, et al.
European Journal of Human Genetics : EJHG|November 28, 2013
Structural genomic variation in childhood epilepsies with complex phenotypesIngo Helbig, Marielle E M Swinkels, Emmelien Aten, et al.
Human Genetics|May 6, 2010
WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterationsKatrin Friedrich, Lin Lee, Dru F Leistritz, et al.
Human Mutation|September 27, 2016
WRN Mutation Update: Mutation Spectrum, Patient Registries, and Translational ProspectsKoutaro Yokote, Sirisak Chanprasert, Lin Lee, et al.
Plos One|June 4, 2009
Gene-network analysis identifies susceptibility genes related to glycobiology in autismBert van der Zwaag, Lude Franke, Martin Poot, et al.
Human Mutation|May 5, 2006
The spectrum of WRN mutations in Werner syndrome patientsShurong Huang, Lin Lee, Nancy B Hanson, et al.
Plos Genetics|February 21, 2012
Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disordersClaire S Leblond, Jutta Heinrich, Richard Delorme, et al.
The New England Journal of Medicine|September 12, 2008
Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypesHeather C Mefford, Andrew J Sharp, Carl Baker, et al.
Pageof 10