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Lisa G Shaffer

Showing results (121-130 of 215) with videos related to

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The Korean Journal of Laboratory Medicine|March 4, 2010
A de novo proximal 6q deletion confirmed by array comparative genomic hybridizationKwang-Sook Woo, Ji-Eun Kim, Kyung-Eun Kim, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 3, 2010
Copy number variations associated with autism spectrum disorders contribute to a spectrum of neurodevelopmental disordersJill A Rosenfeld, Blake C Ballif, Beth S Torchia, et al.
Human Molecular Genetics|February 5, 2013
Contribution of copy number variants involving nonsense-mediated mRNA decay pathway genes to neuro-developmental disordersLam S Nguyen, Hyung-Goo Kim, Jill A Rosenfeld, et al.
European Journal of Human Genetics : EJHG|February 10, 2012
Proximal microdeletions and microduplications of 1q21.1 contribute to variable abnormal phenotypesJill A Rosenfeld, Ryan N Traylor, G Bradley Schaefer, et al.
American Journal of Medical Genetics. Part A|November 22, 2013
Refinement of the 8q22.1 microdeletion critical region associated with Nablus mask-like facial syndromeJustin Overhoff, Marina M Rabideau, Lynne M Bird, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 7, 2012
Defining the impact of maternal cell contamination on the interpretation of prenatal microarray analysisAllen N Lamb, Jill A Rosenfeld, Justine Coppinger, et al.
Human Genetics|April 6, 2002
A case of segmental paternal isodisomy of chromosome 14Karen J Coveler, Sam P Yang, ReidV Sutton, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 7, 2007
Development of a high-density pericentromeric region BAC clone set for the detection and characterization of small supernumerary marker chromosomes by array CGHBlake C Ballif, Sara A Hornor, Scott G Sulpizio, et al.
Prenatal Diagnosis|May 25, 2012
Referral patterns for microarray testing in prenatal diagnosisLisa G Shaffer, Mindy Preston Dabell, Jill A Rosenfeld, et al.
American Journal of Human Genetics|April 11, 2003
Physical map of 1p36, placement of breakpoints in monosomy 1p36, and clinical characterization of the syndromeHeidi A Heilstedt, Blake C Ballif, Leslie A Howard, et al.
Pageof 22

Showing results (121-130 of 215) with videos related to

Sort By:
Pageof 22
The Korean Journal of Laboratory Medicine|March 4, 2010
A de novo proximal 6q deletion confirmed by array comparative genomic hybridizationKwang-Sook Woo, Ji-Eun Kim, Kyung-Eun Kim, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 3, 2010
Copy number variations associated with autism spectrum disorders contribute to a spectrum of neurodevelopmental disordersJill A Rosenfeld, Blake C Ballif, Beth S Torchia, et al.
Human Molecular Genetics|February 5, 2013
Contribution of copy number variants involving nonsense-mediated mRNA decay pathway genes to neuro-developmental disordersLam S Nguyen, Hyung-Goo Kim, Jill A Rosenfeld, et al.
European Journal of Human Genetics : EJHG|February 10, 2012
Proximal microdeletions and microduplications of 1q21.1 contribute to variable abnormal phenotypesJill A Rosenfeld, Ryan N Traylor, G Bradley Schaefer, et al.
American Journal of Medical Genetics. Part A|November 22, 2013
Refinement of the 8q22.1 microdeletion critical region associated with Nablus mask-like facial syndromeJustin Overhoff, Marina M Rabideau, Lynne M Bird, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 7, 2012
Defining the impact of maternal cell contamination on the interpretation of prenatal microarray analysisAllen N Lamb, Jill A Rosenfeld, Justine Coppinger, et al.
Human Genetics|April 6, 2002
A case of segmental paternal isodisomy of chromosome 14Karen J Coveler, Sam P Yang, ReidV Sutton, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 7, 2007
Development of a high-density pericentromeric region BAC clone set for the detection and characterization of small supernumerary marker chromosomes by array CGHBlake C Ballif, Sara A Hornor, Scott G Sulpizio, et al.
Prenatal Diagnosis|May 25, 2012
Referral patterns for microarray testing in prenatal diagnosisLisa G Shaffer, Mindy Preston Dabell, Jill A Rosenfeld, et al.
American Journal of Human Genetics|April 11, 2003
Physical map of 1p36, placement of breakpoints in monosomy 1p36, and clinical characterization of the syndromeHeidi A Heilstedt, Blake C Ballif, Leslie A Howard, et al.
Pageof 22