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Jennifer G Mulle

Showing results (21-30 of 70) with videos related to

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Plos One|April 3, 2010
Empirical evaluation of oligonucleotide probe selection for DNA microarraysJennifer G Mulle, Viren C Patel, Stephen T Warren, et al.
Alcoholism, Clinical and Experimental Research|November 27, 2016
Response to Astley's Letter to the EditorClaire D Coles, Amanda R Gailey, Jennifer G Mulle, et al.
Alcoholism, Clinical and Experimental Research|March 31, 2016
A Comparison Among 5 Methods for the Clinical Diagnosis of Fetal Alcohol Spectrum DisordersClaire D Coles, Amanda R Gailey, Jennifer G Mulle, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 29, 2007
Replication stress induces tumor-like microdeletions in FHIT/FRA3BSandra G Durkin, Ryan L Ragland, Martin F Arlt, et al.
Human Mutation|July 30, 2008
Microarray-based mutation detection in the dystrophin geneMadhuri R Hegde, Ephrem L H Chin, Jennifer G Mulle, et al.
Journal of Neuroscience Research|November 19, 2016
Unraveling the genetic architecture of copy number variants associated with schizophrenia and other neuropsychiatric disordersTimothy P Rutkowski, Jason P Schroeder, Georgette M Gafford, et al.
Journal of Developmental and Behavioral Pediatrics : JDBP|October 12, 2021
Symptoms of Pediatric Feeding Disorders Among Individuals with 3q29 Deletion Syndrome: A Case-Control StudyAddam J Wawrzonek, William Sharp, Teresa Lindsey Burrell, et al.
Molecular Autism|July 27, 2019
Neuropsychiatric phenotypes and a distinct constellation of ASD features in 3q29 deletion syndrome: results from the 3q29 registryRebecca M Pollak, Melissa M Murphy, Michael P Epstein, et al.
American Journal of Medical Genetics. Part A|September 11, 2023
Musculoskeletal phenotypes in 3q29 deletion syndromeRebecca M Pollak, Jacob C Tilmon, Melissa M Murphy, et al.
Medrxiv : the Preprint Server for Health Sciences|April 17, 2023
Musculoskeletal phenotypes in 3q29 deletion syndromeRebecca M Pollak, Jacob C Tilmon, Melissa M Murphy, et al.
Pageof 7

Showing results (21-30 of 70) with videos related to

Sort By:
Pageof 7
Plos One|April 3, 2010
Empirical evaluation of oligonucleotide probe selection for DNA microarraysJennifer G Mulle, Viren C Patel, Stephen T Warren, et al.
Alcoholism, Clinical and Experimental Research|November 27, 2016
Response to Astley's Letter to the EditorClaire D Coles, Amanda R Gailey, Jennifer G Mulle, et al.
Alcoholism, Clinical and Experimental Research|March 31, 2016
A Comparison Among 5 Methods for the Clinical Diagnosis of Fetal Alcohol Spectrum DisordersClaire D Coles, Amanda R Gailey, Jennifer G Mulle, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 29, 2007
Replication stress induces tumor-like microdeletions in FHIT/FRA3BSandra G Durkin, Ryan L Ragland, Martin F Arlt, et al.
Human Mutation|July 30, 2008
Microarray-based mutation detection in the dystrophin geneMadhuri R Hegde, Ephrem L H Chin, Jennifer G Mulle, et al.
Journal of Neuroscience Research|November 19, 2016
Unraveling the genetic architecture of copy number variants associated with schizophrenia and other neuropsychiatric disordersTimothy P Rutkowski, Jason P Schroeder, Georgette M Gafford, et al.
Journal of Developmental and Behavioral Pediatrics : JDBP|October 12, 2021
Symptoms of Pediatric Feeding Disorders Among Individuals with 3q29 Deletion Syndrome: A Case-Control StudyAddam J Wawrzonek, William Sharp, Teresa Lindsey Burrell, et al.
Molecular Autism|July 27, 2019
Neuropsychiatric phenotypes and a distinct constellation of ASD features in 3q29 deletion syndrome: results from the 3q29 registryRebecca M Pollak, Melissa M Murphy, Michael P Epstein, et al.
American Journal of Medical Genetics. Part A|September 11, 2023
Musculoskeletal phenotypes in 3q29 deletion syndromeRebecca M Pollak, Jacob C Tilmon, Melissa M Murphy, et al.
Medrxiv : the Preprint Server for Health Sciences|April 17, 2023
Musculoskeletal phenotypes in 3q29 deletion syndromeRebecca M Pollak, Jacob C Tilmon, Melissa M Murphy, et al.
Pageof 7