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Erik C Thorland

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Molecular Cytogenetics|March 24, 2016
Patients with mosaic methylation patterns of the Prader-Willi/Angelman Syndrome critical region exhibit AS-like phenotypes with some PWS featuresUmut Aypar, Nicole L Hoppman, Erik C Thorland, et al.
Oncogene|February 28, 2003
Common fragile sites are preferential targets for HPV16 integrations in cervical tumorsErik C Thorland, Shannon L Myers, Bobbie S Gostout, et al.
American Journal of Medical Genetics. Part A|September 14, 2007
Evaluation of a commercially available focused aCGH platform for the detection of constitutional chromosome anomaliesBrandon M Shearer, Erik C Thorland, Patrick R Gonzales, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 18, 2011
American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variantsHutton M Kearney, Erik C Thorland, Kerry K Brown, et al.
Genes & Diseases|March 12, 2016
Syndromic craniosynostosis associated with microdeletion of chromosome 19p13.12-19p13.2Sarah M Lyon, Darrel Waggoner, Sara Halbach, et al.
Oncogene|December 17, 2002
Evidence that instability within the FRA3B region extends four megabasesNicole A Becker, Erik C Thorland, Stacy R Denison, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 18, 2007
Comprehensive validation of array comparative genomic hybridization platforms: how much is enough?Erik C Thorland, Patrick R Gonzales, Troy J Gliem, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 19, 2011
Reflex fluorescent in situ hybridization testing for unsuccessful product of conception cultures: a retrospective analysis of 5555 samples attempted by conventional cytogenetics and fluorescent in situ hybridizationBrandon M Shearer, Erik C Thorland, Austin W Carlson, et al.
American Journal of Medical Genetics. Part A|July 1, 2014
Does parent of origin matter? Methylation studies should be performed on patients with multiple copies of the Prader-Willi/Angelman syndrome critical regionUmut Aypar, Pamela R Brodersen, Patrick A Lundquist, et al.
Biochemical and Biophysical Research Communications|December 3, 2005
Congenital disorder of glycosylation Ic due to a de novo deletion and an hALG-6 mutationErik A Eklund, Liangwu Sun, Samuel P Yang, et al.
Pageof 5

Showing results (1-10 of 46) with videos related to

Sort By:
Pageof 5
Molecular Cytogenetics|March 24, 2016
Patients with mosaic methylation patterns of the Prader-Willi/Angelman Syndrome critical region exhibit AS-like phenotypes with some PWS featuresUmut Aypar, Nicole L Hoppman, Erik C Thorland, et al.
Oncogene|February 28, 2003
Common fragile sites are preferential targets for HPV16 integrations in cervical tumorsErik C Thorland, Shannon L Myers, Bobbie S Gostout, et al.
American Journal of Medical Genetics. Part A|September 14, 2007
Evaluation of a commercially available focused aCGH platform for the detection of constitutional chromosome anomaliesBrandon M Shearer, Erik C Thorland, Patrick R Gonzales, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 18, 2011
American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variantsHutton M Kearney, Erik C Thorland, Kerry K Brown, et al.
Genes & Diseases|March 12, 2016
Syndromic craniosynostosis associated with microdeletion of chromosome 19p13.12-19p13.2Sarah M Lyon, Darrel Waggoner, Sara Halbach, et al.
Oncogene|December 17, 2002
Evidence that instability within the FRA3B region extends four megabasesNicole A Becker, Erik C Thorland, Stacy R Denison, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 18, 2007
Comprehensive validation of array comparative genomic hybridization platforms: how much is enough?Erik C Thorland, Patrick R Gonzales, Troy J Gliem, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 19, 2011
Reflex fluorescent in situ hybridization testing for unsuccessful product of conception cultures: a retrospective analysis of 5555 samples attempted by conventional cytogenetics and fluorescent in situ hybridizationBrandon M Shearer, Erik C Thorland, Austin W Carlson, et al.
American Journal of Medical Genetics. Part A|July 1, 2014
Does parent of origin matter? Methylation studies should be performed on patients with multiple copies of the Prader-Willi/Angelman syndrome critical regionUmut Aypar, Pamela R Brodersen, Patrick A Lundquist, et al.
Biochemical and Biophysical Research Communications|December 3, 2005
Congenital disorder of glycosylation Ic due to a de novo deletion and an hALG-6 mutationErik A Eklund, Liangwu Sun, Samuel P Yang, et al.
Pageof 5