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Robert E Pyatt

Showing results (1-10 of 22) with videos related to

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Clinics in Laboratory Medicine|November 29, 2011
Interpretation of copy number alterations identified through clinical microarray-comparative genomic hybridizationRobert E Pyatt, Caroline Astbury
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 18, 2006
A feasibility study for the newborn screening of spinal muscular atrophyRobert E Pyatt, Thomas W Prior
The Journal of Molecular Diagnostics : JMD|January 27, 2006
Mutation screening in juvenile polyposis syndromeRobert E Pyatt, Robert Pilarski, Thomas W Prior
Clinical Chemistry|September 25, 2007
Assessment of liquid microbead arrays for the screening of newborns for spinal muscular atrophyRobert E Pyatt, David C Mihal, Thomas W Prior
Journal of Genetic Counseling|October 8, 2020
Impact of variant reclassification in the clinical setting of cardiovascular geneticsRebecca E VanDyke, Sayaka Hashimoto, Ana Morales, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|October 10, 2014
Complex brain malformations associated with chromosome 6q27 gain that includes THBS2, which encodes thrombospondin 2, an astrocyte-derived protein of the extracellular matrixMelissa N Burnside, Robert E Pyatt, Anna Hughes, et al.
Journal of Health Communication|May 8, 2019
Understanding <i>BRCA</i> Mutation Carriers' Preferences for Communication of Genetic Modifiers of Breast Cancer RiskShelly R Hovick, Naomi Tan, Lindsey Morr, et al.
European Journal of Medical Genetics|July 31, 2013
Multigeneration family with short stature, developmental delay, and dysmorphic features due to 4q27-q28.1 microdeletionScott E Hickey, Sawona Biswas, Devon Lamb Thrush, et al.
Molecular Genetics & Genomic Medicine|March 25, 2015
Variability in pathogenicity prediction programs: impact on clinical diagnosticsLauren C Walters-Sen, Sayaka Hashimoto, Devon Lamb Thrush, et al.
American Journal of Medical Genetics. Part A|March 23, 2017
Partial tetrasomy 11q resulting from an intrachromosomal triplication of a 22 Mb region of chromosome 11Mariana Kekis, Carol Deeg, Sayaka Hashimoto, et al.
Pageof 3

Showing results (1-10 of 22) with videos related to

Sort By:
Pageof 3
Clinics in Laboratory Medicine|November 29, 2011
Interpretation of copy number alterations identified through clinical microarray-comparative genomic hybridizationRobert E Pyatt, Caroline Astbury
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 18, 2006
A feasibility study for the newborn screening of spinal muscular atrophyRobert E Pyatt, Thomas W Prior
The Journal of Molecular Diagnostics : JMD|January 27, 2006
Mutation screening in juvenile polyposis syndromeRobert E Pyatt, Robert Pilarski, Thomas W Prior
Clinical Chemistry|September 25, 2007
Assessment of liquid microbead arrays for the screening of newborns for spinal muscular atrophyRobert E Pyatt, David C Mihal, Thomas W Prior
Journal of Genetic Counseling|October 8, 2020
Impact of variant reclassification in the clinical setting of cardiovascular geneticsRebecca E VanDyke, Sayaka Hashimoto, Ana Morales, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|October 10, 2014
Complex brain malformations associated with chromosome 6q27 gain that includes THBS2, which encodes thrombospondin 2, an astrocyte-derived protein of the extracellular matrixMelissa N Burnside, Robert E Pyatt, Anna Hughes, et al.
Journal of Health Communication|May 8, 2019
Understanding <i>BRCA</i> Mutation Carriers' Preferences for Communication of Genetic Modifiers of Breast Cancer RiskShelly R Hovick, Naomi Tan, Lindsey Morr, et al.
European Journal of Medical Genetics|July 31, 2013
Multigeneration family with short stature, developmental delay, and dysmorphic features due to 4q27-q28.1 microdeletionScott E Hickey, Sawona Biswas, Devon Lamb Thrush, et al.
Molecular Genetics & Genomic Medicine|March 25, 2015
Variability in pathogenicity prediction programs: impact on clinical diagnosticsLauren C Walters-Sen, Sayaka Hashimoto, Devon Lamb Thrush, et al.
American Journal of Medical Genetics. Part A|March 23, 2017
Partial tetrasomy 11q resulting from an intrachromosomal triplication of a 22 Mb region of chromosome 11Mariana Kekis, Carol Deeg, Sayaka Hashimoto, et al.
Pageof 3