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Nigel P Carter

Showing results (71-80 of 104) with videos related to

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Mammalian Genome : Official Journal of the International Mammalian Genome Society|March 21, 2003
Construction and integration of radiation-hybrid and cytogenetic maps of dog Chromosome XHelen F Spriggs, Nigel G Holmes, Matthew G Breen, et al.
American Journal of Human Genetics|December 29, 2005
Heterogeneous duplications in patients with Pelizaeus-Merzbacher disease suggest a mechanism of coupled homologous and nonhomologous recombinationKaren J Woodward, Maria Cundall, Karen Sperle, et al.
Biochemical Society Transactions|March 20, 2010
Confirmed rare copy number variants implicate novel genes in schizophreniaGloria W C Tam, Louie N van de Lagemaat, Richard Redon, et al.
American Journal of Medical Genetics. Part A|September 29, 2011
Maternally inherited partial monosomy 9p (pter → p24.1) and partial trisomy 20p (pter → p12.1) characterized by microarray comparative genomic hybridizationÉrika L Freitas, Susan M Gribble, Milena Simioni, et al.
Genes, Chromosomes & Cancer|January 6, 2007
Characterization of a 3;6 translocation associated with renal cell carcinomaRebecca E Foster, Mahera Abdulrahman, Mark R Morris, et al.
American Journal of Human Genetics|August 3, 2010
Distinct effects of allelic NFIX mutations on nonsense-mediated mRNA decay engender either a Sotos-like or a Marshall-Smith syndromeValérie Malan, Diana Rajan, Sophie Thomas, et al.
Nature|May 15, 2007
Completing the map of human genetic variation, Evan E Eichler, Deborah A Nickerson, et al.
Human Mutation|August 20, 2015
Diagnostic interpretation of array data using public databases and internet sourcesNicole de Leeuw, Trijnie Dijkhuizen, Jayne Y Hehir-Kwa, et al.
Nature Genetics|October 7, 2008
EYS, encoding an ortholog of Drosophila spacemaker, is mutated in autosomal recessive retinitis pigmentosaMai M Abd El-Aziz, Isabel Barragan, Ciara A O'Driscoll, et al.
Journal of Medical Genetics|February 1, 2011
High incidence of recurrent copy number variants in patients with isolated and syndromic Müllerian aplasiaSerena Nik-Zainal, Reiner Strick, Mekayla Storer, et al.
Pageof 11

Showing results (71-80 of 104) with videos related to

Sort By:
Pageof 11
Mammalian Genome : Official Journal of the International Mammalian Genome Society|March 21, 2003
Construction and integration of radiation-hybrid and cytogenetic maps of dog Chromosome XHelen F Spriggs, Nigel G Holmes, Matthew G Breen, et al.
American Journal of Human Genetics|December 29, 2005
Heterogeneous duplications in patients with Pelizaeus-Merzbacher disease suggest a mechanism of coupled homologous and nonhomologous recombinationKaren J Woodward, Maria Cundall, Karen Sperle, et al.
Biochemical Society Transactions|March 20, 2010
Confirmed rare copy number variants implicate novel genes in schizophreniaGloria W C Tam, Louie N van de Lagemaat, Richard Redon, et al.
American Journal of Medical Genetics. Part A|September 29, 2011
Maternally inherited partial monosomy 9p (pter → p24.1) and partial trisomy 20p (pter → p12.1) characterized by microarray comparative genomic hybridizationÉrika L Freitas, Susan M Gribble, Milena Simioni, et al.
Genes, Chromosomes & Cancer|January 6, 2007
Characterization of a 3;6 translocation associated with renal cell carcinomaRebecca E Foster, Mahera Abdulrahman, Mark R Morris, et al.
American Journal of Human Genetics|August 3, 2010
Distinct effects of allelic NFIX mutations on nonsense-mediated mRNA decay engender either a Sotos-like or a Marshall-Smith syndromeValérie Malan, Diana Rajan, Sophie Thomas, et al.
Nature|May 15, 2007
Completing the map of human genetic variation, Evan E Eichler, Deborah A Nickerson, et al.
Human Mutation|August 20, 2015
Diagnostic interpretation of array data using public databases and internet sourcesNicole de Leeuw, Trijnie Dijkhuizen, Jayne Y Hehir-Kwa, et al.
Nature Genetics|October 7, 2008
EYS, encoding an ortholog of Drosophila spacemaker, is mutated in autosomal recessive retinitis pigmentosaMai M Abd El-Aziz, Isabel Barragan, Ciara A O'Driscoll, et al.
Journal of Medical Genetics|February 1, 2011
High incidence of recurrent copy number variants in patients with isolated and syndromic Müllerian aplasiaSerena Nik-Zainal, Reiner Strick, Mekayla Storer, et al.
Pageof 11