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G Brunner

Showing results (411-420 of 727) with videos related to

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Genomics Data|August 11, 2015
Platform comparison of detecting copy number variants with microarrays and whole-exome sequencingJoep de Ligt, Philip M Boone, Rolph Pfundt, et al.
American Journal of Human Genetics|April 16, 2002
High-throughput analysis of subtelomeric chromosome rearrangements by use of array-based comparative genomic hybridizationJoris A Veltman, Eric F P M Schoenmakers, Bert H Eussen, et al.
Molecular Syndromology|July 22, 2010
Severe Progressive Autism Associated with Two de novo Changes: A 2.6-Mb 2q31.1 Deletion and a Balanced t(14;21)(q21.1;p11.2) Translocation with Long-Range Epigenetic Silencing of LRFN5 ExpressionD R H de Bruijn, A H A van Dijk, R Pfundt, et al.
Plos One|April 28, 2012
Nonuniform cardiac denervation observed by 11C-meta-hydroxyephedrine PET in 6-OHDA-treated monkeysValerie Joers, Kailie Seneczko, Nichole C Goecks, et al.
Human Molecular Genetics|August 1, 1994
Mutations in the type IV collagen alpha 3 (COL4A3) gene in autosomal recessive Alport syndromeH H Lemmink, T Mochizuki, L P van den Heuvel, et al.
Epidemiology (Cambridge, Mass.)|January 8, 2015
Parental subfertility, fertility treatment, and the risk of congenital anorectal malformationsCharlotte H W Wijers, Iris A L M van Rooij, Roxana Rassouli, et al.
Transplantation|August 19, 2003
Immunotoxin-treated rhesus monkeys: a model for renal allograft chronic rejectionJose R Torrealba, Luis A Fernandez, Turan Kanmaz, et al.
European Journal of Human Genetics : EJHG|October 23, 2003
No evidence for involvement of IL-4R and CD11B from the IBD1 region and STAT6 in the IBD2 region in Crohn's diseaseDirk J de Jong, Barbara Franke, Anton H J Naber, et al.
American Journal of Human Genetics|March 31, 2015
Mutations in DVL1 cause an osteosclerotic form of Robinow syndromeKieran J Bunn, Phil Daniel, Heleen S Rösken, et al.
Journal of Medical Genetics|December 1, 1992
Linkage analysis with chromosome 15q11-13 markers shows genomic imprinting in familial Angelman syndromeE J Meijers-Heijboer, L A Sandkuijl, H G Brunner, et al.
Pageof 73

Showing results (411-420 of 727) with videos related to

Sort By:
Pageof 73
Genomics Data|August 11, 2015
Platform comparison of detecting copy number variants with microarrays and whole-exome sequencingJoep de Ligt, Philip M Boone, Rolph Pfundt, et al.
American Journal of Human Genetics|April 16, 2002
High-throughput analysis of subtelomeric chromosome rearrangements by use of array-based comparative genomic hybridizationJoris A Veltman, Eric F P M Schoenmakers, Bert H Eussen, et al.
Molecular Syndromology|July 22, 2010
Severe Progressive Autism Associated with Two de novo Changes: A 2.6-Mb 2q31.1 Deletion and a Balanced t(14;21)(q21.1;p11.2) Translocation with Long-Range Epigenetic Silencing of LRFN5 ExpressionD R H de Bruijn, A H A van Dijk, R Pfundt, et al.
Plos One|April 28, 2012
Nonuniform cardiac denervation observed by 11C-meta-hydroxyephedrine PET in 6-OHDA-treated monkeysValerie Joers, Kailie Seneczko, Nichole C Goecks, et al.
Human Molecular Genetics|August 1, 1994
Mutations in the type IV collagen alpha 3 (COL4A3) gene in autosomal recessive Alport syndromeH H Lemmink, T Mochizuki, L P van den Heuvel, et al.
Epidemiology (Cambridge, Mass.)|January 8, 2015
Parental subfertility, fertility treatment, and the risk of congenital anorectal malformationsCharlotte H W Wijers, Iris A L M van Rooij, Roxana Rassouli, et al.
Transplantation|August 19, 2003
Immunotoxin-treated rhesus monkeys: a model for renal allograft chronic rejectionJose R Torrealba, Luis A Fernandez, Turan Kanmaz, et al.
European Journal of Human Genetics : EJHG|October 23, 2003
No evidence for involvement of IL-4R and CD11B from the IBD1 region and STAT6 in the IBD2 region in Crohn's diseaseDirk J de Jong, Barbara Franke, Anton H J Naber, et al.
American Journal of Human Genetics|March 31, 2015
Mutations in DVL1 cause an osteosclerotic form of Robinow syndromeKieran J Bunn, Phil Daniel, Heleen S Rösken, et al.
Journal of Medical Genetics|December 1, 1992
Linkage analysis with chromosome 15q11-13 markers shows genomic imprinting in familial Angelman syndromeE J Meijers-Heijboer, L A Sandkuijl, H G Brunner, et al.
Pageof 73