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Laura Russell

Showing results (41-50 of 48) with videos related to

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Plos Genetics|July 13, 2018
Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birthJohanna M Huusko, Minna K Karjalainen, Britney E Graham, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 23, 2017
Opinion: Why we need a centralized repository for isotopic dataJonathan N Pauli, Seth D Newsome, Joseph A Cook, et al.
Plos Genetics|September 14, 2018
Correction: Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birthJohanna M Huusko, Minna K Karjalainen, Britney E Graham, et al.
Journal of Clinical Child and Adolescent Psychology : the Official Journal for the Society of Clinical Child and Adolescent Psychology, American Psychological Association, Division 53|May 8, 2020
A Clinical Program for Transgender and Gender-Diverse Neurodiverse/Autistic Adolescents Developed through Community-Based Participatory DesignJohn F Strang, Megan Knauss, Anna van der Miesen, et al.
Annals of Clinical and Translational Neurology|December 10, 2019
RARS1-related hypomyelinating leukodystrophy: Expanding the spectrumMarisa I Mendes, Lydia M C Green, Enrico Bertini, et al.
The New England Journal of Medicine|September 7, 2017
Genetic Associations with Gestational Duration and Spontaneous Preterm BirthGe Zhang, Bjarke Feenstra, Jonas Bacelis, et al.
American Journal of Human Genetics|January 2, 2018
Genotype-Phenotype Correlation in NF1: Evidence for a More Severe Phenotype Associated with Missense Mutations Affecting NF1 Codons 844-848Magdalena Koczkowska, Yunjia Chen, Tom Callens, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 4, 2019
Widening of the genetic and clinical spectrum of Lamb-Shaffer syndrome, a neurodevelopmental disorder due to SOX5 haploinsufficiencyAsh Zawerton, Cyril Mignot, Ashley Sigafoos, et al.
Pageof 5

Showing results (41-50 of 48) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 48 results.
Plos Genetics|July 13, 2018
Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birthJohanna M Huusko, Minna K Karjalainen, Britney E Graham, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 23, 2017
Opinion: Why we need a centralized repository for isotopic dataJonathan N Pauli, Seth D Newsome, Joseph A Cook, et al.
Plos Genetics|September 14, 2018
Correction: Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birthJohanna M Huusko, Minna K Karjalainen, Britney E Graham, et al.
Journal of Clinical Child and Adolescent Psychology : the Official Journal for the Society of Clinical Child and Adolescent Psychology, American Psychological Association, Division 53|May 8, 2020
A Clinical Program for Transgender and Gender-Diverse Neurodiverse/Autistic Adolescents Developed through Community-Based Participatory DesignJohn F Strang, Megan Knauss, Anna van der Miesen, et al.
Annals of Clinical and Translational Neurology|December 10, 2019
RARS1-related hypomyelinating leukodystrophy: Expanding the spectrumMarisa I Mendes, Lydia M C Green, Enrico Bertini, et al.
The New England Journal of Medicine|September 7, 2017
Genetic Associations with Gestational Duration and Spontaneous Preterm BirthGe Zhang, Bjarke Feenstra, Jonas Bacelis, et al.
American Journal of Human Genetics|January 2, 2018
Genotype-Phenotype Correlation in NF1: Evidence for a More Severe Phenotype Associated with Missense Mutations Affecting NF1 Codons 844-848Magdalena Koczkowska, Yunjia Chen, Tom Callens, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 4, 2019
Widening of the genetic and clinical spectrum of Lamb-Shaffer syndrome, a neurodevelopmental disorder due to SOX5 haploinsufficiencyAsh Zawerton, Cyril Mignot, Ashley Sigafoos, et al.
Pageof 5