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Greg B Peters

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Methods in Molecular Biology (Clifton, N.J.)|May 30, 2014
Chromosome microarrays in diagnostic testing: interpreting the genomic dataGreg B Peters, Mark D Pertile
Journal of Paediatrics and Child Health|February 11, 2012
Chromosome microarray in Australia: a guide for paediatriciansElizabeth E Palmer, Greg B Peters, David Mowat
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|April 22, 2006
Chromosome microdissection identifies genomic amplifications associated with drug resistance in a leukemia cell line: an approach to understanding drug resistance in cancerFrouzandeh Mahjoubi, Ronald J Hill, Greg B Peters
Movement Disorders : Official Journal of the Movement Disorder Society|March 23, 2011
Familial 7q21.3 microdeletion involving epsilon-sarcoglycan causing myoclonus dystonia, cognitive impairment, and psychosisRussell C Dale, Julian J Nasti, Greg B Peters
Pathology|July 17, 2010
Fibrosarcomatous variant of dermatofibrosarcoma protuberans showing COL1A1-PDGFB gene fusion, detected using a novel and disease-specific RT-PCR protocolHema Mahajan, Raghwa Sharma, Artur Darmanian, et al.
Developmental Medicine and Child Neurology|April 21, 2012
Microdeletions detected using chromosome microarray in children with suspected genetic movement disorders: a single-centre studyRussell C Dale, Padraic Grattan-Smith, Michelle Nicholson, et al.
Neurology|September 24, 2011
Infantile convulsions and paroxysmal kinesigenic dyskinesia with 16p11.2 microdeletionRussell C Dale, Padraic Grattan-Smith, Victor S C Fung, et al.
Cancer Research|February 28, 2007
Paternally inherited submicroscopic duplication at 11p15.5 implicates insulin-like growth factor II in overgrowth and Wilms' tumorigenesisElizabeth M Algar, Luke St Heaps, Artur Darmanian, et al.
European Journal of Human Genetics : EJHG|November 27, 2014
Deletion of protein tyrosine phosphatase, non-receptor type 4 (PTPN4) in twins with a Rett syndrome-like phenotypeSarah L Williamson, Carolyn J Ellaway, Greg B Peters, et al.
Clinical Genetics|January 23, 2023
Further delineation of dosage-sensitive K/L mediated Xq28 duplication syndrome includes incomplete penetranceMelanie Leffler, Louise Christie, Anna Hackett, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Methods in Molecular Biology (Clifton, N.J.)|May 30, 2014
Chromosome microarrays in diagnostic testing: interpreting the genomic dataGreg B Peters, Mark D Pertile
Journal of Paediatrics and Child Health|February 11, 2012
Chromosome microarray in Australia: a guide for paediatriciansElizabeth E Palmer, Greg B Peters, David Mowat
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|April 22, 2006
Chromosome microdissection identifies genomic amplifications associated with drug resistance in a leukemia cell line: an approach to understanding drug resistance in cancerFrouzandeh Mahjoubi, Ronald J Hill, Greg B Peters
Movement Disorders : Official Journal of the Movement Disorder Society|March 23, 2011
Familial 7q21.3 microdeletion involving epsilon-sarcoglycan causing myoclonus dystonia, cognitive impairment, and psychosisRussell C Dale, Julian J Nasti, Greg B Peters
Pathology|July 17, 2010
Fibrosarcomatous variant of dermatofibrosarcoma protuberans showing COL1A1-PDGFB gene fusion, detected using a novel and disease-specific RT-PCR protocolHema Mahajan, Raghwa Sharma, Artur Darmanian, et al.
Developmental Medicine and Child Neurology|April 21, 2012
Microdeletions detected using chromosome microarray in children with suspected genetic movement disorders: a single-centre studyRussell C Dale, Padraic Grattan-Smith, Michelle Nicholson, et al.
Neurology|September 24, 2011
Infantile convulsions and paroxysmal kinesigenic dyskinesia with 16p11.2 microdeletionRussell C Dale, Padraic Grattan-Smith, Victor S C Fung, et al.
Cancer Research|February 28, 2007
Paternally inherited submicroscopic duplication at 11p15.5 implicates insulin-like growth factor II in overgrowth and Wilms' tumorigenesisElizabeth M Algar, Luke St Heaps, Artur Darmanian, et al.
European Journal of Human Genetics : EJHG|November 27, 2014
Deletion of protein tyrosine phosphatase, non-receptor type 4 (PTPN4) in twins with a Rett syndrome-like phenotypeSarah L Williamson, Carolyn J Ellaway, Greg B Peters, et al.
Clinical Genetics|January 23, 2023
Further delineation of dosage-sensitive K/L mediated Xq28 duplication syndrome includes incomplete penetranceMelanie Leffler, Louise Christie, Anna Hackett, et al.
Pageof 2