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Carl Dobkin

Showing results (21-30 of 26) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 12, 2014
Fragile X full mutation expansions are inhibited by one or more AGG interruptions in premutation carriersSarah L Nolin, Anne Glicksman, Nicole Ersalesi, et al.
BMC Medical Genetics|October 29, 2014
Fragile X protein in newborn dried blood spotsTatyana Adayev, Giuseppe LaFauci, Carl Dobkin, et al.
Human Mutation|September 17, 2014
Identification of fragile X syndrome specific molecular markers in human fibroblasts: a useful model to test the efficacy of therapeutic drugsDaman Kumari, Aditi Bhattacharya, Jeffrey Nadel, et al.
American Journal of Medical Genetics. Part A|May 4, 2019
Expansions and contractions of the FMR1 CGG repeat in 5,508 transmissions of normal, intermediate, and premutation allelesSarah L Nolin, Anne Glicksman, Nicole Tortora, et al.
American Journal of Medical Genetics. Part A|February 28, 2013
Fragile X AGG analysis provides new risk predictions for 45-69 repeat allelesSarah L Nolin, Sachin Sah, Anne Glicksman, et al.
Brain Sciences|October 3, 2020
A Genotype-Phenotype Study of High-Resolution <i>FMR1</i> Nucleic Acid and Protein Analyses in Fragile X Patients with Neurobehavioral AssessmentsDejan B Budimirovic, Annette Schlageter, Stela Filipovic-Sadic, et al.
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Showing results (21-30 of 26) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 26 results.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 12, 2014
Fragile X full mutation expansions are inhibited by one or more AGG interruptions in premutation carriersSarah L Nolin, Anne Glicksman, Nicole Ersalesi, et al.
BMC Medical Genetics|October 29, 2014
Fragile X protein in newborn dried blood spotsTatyana Adayev, Giuseppe LaFauci, Carl Dobkin, et al.
Human Mutation|September 17, 2014
Identification of fragile X syndrome specific molecular markers in human fibroblasts: a useful model to test the efficacy of therapeutic drugsDaman Kumari, Aditi Bhattacharya, Jeffrey Nadel, et al.
American Journal of Medical Genetics. Part A|May 4, 2019
Expansions and contractions of the FMR1 CGG repeat in 5,508 transmissions of normal, intermediate, and premutation allelesSarah L Nolin, Anne Glicksman, Nicole Tortora, et al.
American Journal of Medical Genetics. Part A|February 28, 2013
Fragile X AGG analysis provides new risk predictions for 45-69 repeat allelesSarah L Nolin, Sachin Sah, Anne Glicksman, et al.
Brain Sciences|October 3, 2020
A Genotype-Phenotype Study of High-Resolution <i>FMR1</i> Nucleic Acid and Protein Analyses in Fragile X Patients with Neurobehavioral AssessmentsDejan B Budimirovic, Annette Schlageter, Stela Filipovic-Sadic, et al.
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