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Devon Lamb Thrush

Showing results (11-20 of 17) with videos related to

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American Journal of Medical Genetics. Part A|July 13, 2012
Microarray comparative genomic hybridization and cytogenetic characterization of tissue-specific mosaicism in three patientsElena A Repnikova, Caroline Astbury, Shalini C Reshmi, et al.
Forensic Science International. Genetics|August 17, 2013
Characterization of copy number variation in genomic regions containing STR loci using array comparative genomic hybridizationElena A Repnikova, Jill A Rosenfeld, Andrea Bailes, et al.
American Journal of Medical Genetics. Part A|August 5, 2010
Unexpected detection of dystrophin gene deletions by array comparative genomic hybridizationCatherine E Cottrell, Thomas W Prior, Robert Pyatt, et al.
American Journal of Human Genetics|March 9, 2010
Identification of a recurrent microdeletion at 17q23.1q23.2 flanked by segmental duplications associated with heart defects and limb abnormalitiesBlake C Ballif, Aaron Theisen, Jill A Rosenfeld, et al.
American Journal of Human Genetics|October 11, 2011
Assessment of 2q23.1 microdeletion syndrome implicates MBD5 as a single causal locus of intellectual disability, epilepsy, and autism spectrum disorderMichael E Talkowski, Sureni V Mullegama, Jill A Rosenfeld, et al.
American Journal of Human Genetics|January 22, 2013
Exonic deletions in AUTS2 cause a syndromic form of intellectual disability and suggest a critical role for the C terminusGea Beunders, Els Voorhoeve, Christelle Golzio, et al.
Genome Biology|March 27, 2014
An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY ChallengeCatherine A Brownstein, Alan H Beggs, Nils Homer, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
American Journal of Medical Genetics. Part A|July 13, 2012
Microarray comparative genomic hybridization and cytogenetic characterization of tissue-specific mosaicism in three patientsElena A Repnikova, Caroline Astbury, Shalini C Reshmi, et al.
Forensic Science International. Genetics|August 17, 2013
Characterization of copy number variation in genomic regions containing STR loci using array comparative genomic hybridizationElena A Repnikova, Jill A Rosenfeld, Andrea Bailes, et al.
American Journal of Medical Genetics. Part A|August 5, 2010
Unexpected detection of dystrophin gene deletions by array comparative genomic hybridizationCatherine E Cottrell, Thomas W Prior, Robert Pyatt, et al.
American Journal of Human Genetics|March 9, 2010
Identification of a recurrent microdeletion at 17q23.1q23.2 flanked by segmental duplications associated with heart defects and limb abnormalitiesBlake C Ballif, Aaron Theisen, Jill A Rosenfeld, et al.
American Journal of Human Genetics|October 11, 2011
Assessment of 2q23.1 microdeletion syndrome implicates MBD5 as a single causal locus of intellectual disability, epilepsy, and autism spectrum disorderMichael E Talkowski, Sureni V Mullegama, Jill A Rosenfeld, et al.
American Journal of Human Genetics|January 22, 2013
Exonic deletions in AUTS2 cause a syndromic form of intellectual disability and suggest a critical role for the C terminusGea Beunders, Els Voorhoeve, Christelle Golzio, et al.
Genome Biology|March 27, 2014
An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY ChallengeCatherine A Brownstein, Alan H Beggs, Nils Homer, et al.
Pageof 2