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Showing results (101-110 of 110) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|January 7, 2015
Independent role for presynaptic FMRP revealed by an FMR1 missense mutation associated with intellectual disability and seizuresLeila K Myrick, Pan-Yue Deng, Hideharu Hashimoto, et al.
Journal of the American Academy of Dermatology|May 26, 2026
Staging imaging reveals clinically significant comorbidities in primary cutaneous marginal zone lymphoma: A retrospective studySara Suhl, Maggie H Zhou, Alexander Kaminsky, et al.
Hereditary Cancer in Clinical Practice|January 9, 2018
Evaluation of a 27-gene inherited cancer panel across 630 consecutive patients referred for testing in a clinical diagnostic laboratorySabrina A Gardner, Katelyn S Weymouth, Wei S Kelly, et al.
Journal of Occupational and Environmental Medicine|July 26, 2016
Relationship Between Changes in Workplace Bullying Status and the Reporting of Personality CharacteristicsRoger Persson, Annie Høgh, Matias Brødsgaard Grynderup, et al.
Birth Defects Research|June 18, 2024
Maternal periconceptional exposure to drinking water disinfection by-products and neural tube defects in offspringV Kancherla, A Rhoads, K M Conway, et al.
Birth Defects Research|November 12, 2022
Influenza vaccination during pregnancy and risk of selected major structural congenital heart defects, National Birth Defects Prevention Study 2006-2011Kristin Palmsten, Jonathan Suhl, Kristin M Conway, et al.
Cancers|September 13, 2025
An Update on Single-Cell RNA Sequencing in Illuminating Disease Mechanisms of Cutaneous T-Cell LymphomaSara Suhl, Alexander Kaminsky, Caroline Chen, et al.
Birth Defects Research|August 23, 2018
Drinking water disinfection byproducts and risk of orofacial clefts in the National Birth Defects Prevention StudyPeter Weyer, Anthony Rhoads, Jonathan Suhl, et al.
Human Genome Variation|June 9, 2016
A catalog of hemizygous variation in 127 22q11 deletion patientsMatthew S Hestand, Beata A Nowakowska, Elfi Vergaelen, et al.
Journal of Medical Genetics|December 13, 2012
Hemizygous mutations in SNAP29 unmask autosomal recessive conditions and contribute to atypical findings in patients with 22q11.2DSDonna M McDonald-McGinn, Somayyeh Fahiminiya, Timothée Revil, et al.
Pageof 11

Showing results (101-110 of 110) with videos related to

Sort By:
Pageof 11
You have reached the last page of results.This site can display upto 110 results.
Proceedings of the National Academy of Sciences of the United States of America|January 7, 2015
Independent role for presynaptic FMRP revealed by an FMR1 missense mutation associated with intellectual disability and seizuresLeila K Myrick, Pan-Yue Deng, Hideharu Hashimoto, et al.
Journal of the American Academy of Dermatology|May 26, 2026
Staging imaging reveals clinically significant comorbidities in primary cutaneous marginal zone lymphoma: A retrospective studySara Suhl, Maggie H Zhou, Alexander Kaminsky, et al.
Hereditary Cancer in Clinical Practice|January 9, 2018
Evaluation of a 27-gene inherited cancer panel across 630 consecutive patients referred for testing in a clinical diagnostic laboratorySabrina A Gardner, Katelyn S Weymouth, Wei S Kelly, et al.
Journal of Occupational and Environmental Medicine|July 26, 2016
Relationship Between Changes in Workplace Bullying Status and the Reporting of Personality CharacteristicsRoger Persson, Annie Høgh, Matias Brødsgaard Grynderup, et al.
Birth Defects Research|June 18, 2024
Maternal periconceptional exposure to drinking water disinfection by-products and neural tube defects in offspringV Kancherla, A Rhoads, K M Conway, et al.
Birth Defects Research|November 12, 2022
Influenza vaccination during pregnancy and risk of selected major structural congenital heart defects, National Birth Defects Prevention Study 2006-2011Kristin Palmsten, Jonathan Suhl, Kristin M Conway, et al.
Cancers|September 13, 2025
An Update on Single-Cell RNA Sequencing in Illuminating Disease Mechanisms of Cutaneous T-Cell LymphomaSara Suhl, Alexander Kaminsky, Caroline Chen, et al.
Birth Defects Research|August 23, 2018
Drinking water disinfection byproducts and risk of orofacial clefts in the National Birth Defects Prevention StudyPeter Weyer, Anthony Rhoads, Jonathan Suhl, et al.
Human Genome Variation|June 9, 2016
A catalog of hemizygous variation in 127 22q11 deletion patientsMatthew S Hestand, Beata A Nowakowska, Elfi Vergaelen, et al.
Journal of Medical Genetics|December 13, 2012
Hemizygous mutations in SNAP29 unmask autosomal recessive conditions and contribute to atypical findings in patients with 22q11.2DSDonna M McDonald-McGinn, Somayyeh Fahiminiya, Timothée Revil, et al.
Pageof 11