Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Lacey A Smith

Showing results (1-10 of 8) with videos related to

Pageof 1
Sort By:
Journal of Genetic Counseling|November 19, 2014
Reporting Incidental Findings in Clinical Whole Exome Sequencing: Incorporation of the 2013 ACMG Recommendations into Current Practices of Genetic CounselingLacey A Smith, Jessica Douglas, Alicia A Braxton, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|August 2, 2011
RUNX transcription factors: association with pediatric asthma and modulated by maternal smokingKathleen J Haley, Jessica Lasky-Su, Sara E Manoli, et al.
Journal of Child Neurology|January 7, 2017
A Model Program for Translational Medicine in Epilepsy GeneticsLacey A Smith, Jeremy F P Ullmann, Heather E Olson, et al.
Respiratory Research|June 2, 2012
Maternal smoking and the retinoid pathway in the developing lungSara E Manoli, Lacey A Smith, Carrie A Vyhlidal, et al.
American Journal of Human Genetics|April 17, 2018
A Recurrent De Novo PACS2 Heterozygous Missense Variant Causes Neonatal-Onset Developmental Epileptic Encephalopathy, Facial Dysmorphism, and Cerebellar DysgenesisHeather E Olson, Nolwenn Jean-Marçais, Edward Yang, et al.
American Journal of Human Genetics|October 6, 2018
A Recurrent De Novo PACS2 Heterozygous Missense Variant Causes Neonatal-Onset Developmental Epileptic Encephalopathy, Facial Dysmorphism, and Cerebellar DysgenesisHeather E Olson, Nolwenn Jean-Marçais, Edward Yang, et al.
American Journal of Human Genetics|March 9, 2019
De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and DyskinesiasKatherine L Helbig, Robert J Lauerer, Jacqueline C Bahr, et al.
American Journal of Human Genetics|October 23, 2018
De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and DyskinesiasKatherine L Helbig, Robert J Lauerer, Jacqueline C Bahr, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Journal of Genetic Counseling|November 19, 2014
Reporting Incidental Findings in Clinical Whole Exome Sequencing: Incorporation of the 2013 ACMG Recommendations into Current Practices of Genetic CounselingLacey A Smith, Jessica Douglas, Alicia A Braxton, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|August 2, 2011
RUNX transcription factors: association with pediatric asthma and modulated by maternal smokingKathleen J Haley, Jessica Lasky-Su, Sara E Manoli, et al.
Journal of Child Neurology|January 7, 2017
A Model Program for Translational Medicine in Epilepsy GeneticsLacey A Smith, Jeremy F P Ullmann, Heather E Olson, et al.
Respiratory Research|June 2, 2012
Maternal smoking and the retinoid pathway in the developing lungSara E Manoli, Lacey A Smith, Carrie A Vyhlidal, et al.
American Journal of Human Genetics|April 17, 2018
A Recurrent De Novo PACS2 Heterozygous Missense Variant Causes Neonatal-Onset Developmental Epileptic Encephalopathy, Facial Dysmorphism, and Cerebellar DysgenesisHeather E Olson, Nolwenn Jean-Marçais, Edward Yang, et al.
American Journal of Human Genetics|October 6, 2018
A Recurrent De Novo PACS2 Heterozygous Missense Variant Causes Neonatal-Onset Developmental Epileptic Encephalopathy, Facial Dysmorphism, and Cerebellar DysgenesisHeather E Olson, Nolwenn Jean-Marçais, Edward Yang, et al.
American Journal of Human Genetics|March 9, 2019
De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and DyskinesiasKatherine L Helbig, Robert J Lauerer, Jacqueline C Bahr, et al.
American Journal of Human Genetics|October 23, 2018
De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and DyskinesiasKatherine L Helbig, Robert J Lauerer, Jacqueline C Bahr, et al.
Pageof 1