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M Shively

Showing results (81-90 of 94) with videos related to

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Mammalian Genome : Official Journal of the International Mammalian Genome Society|August 17, 2013
Multiple mutant T alleles cause haploinsufficiency of Brachyury and short tails in Manx catsKati J Buckingham, Margaret J McMillin, Margaret M Brassil, et al.
Current Microbiology|January 10, 2003
Organization of carboxysome genes in the thiobacilliGordon C Cannon, Stefanie H Baker, Ferda Soyer, et al.
Genes, Brain, and Behavior|October 19, 2017
Variants regulating ZBTB4 are associated with age-at-onset of Alzheimer's diseaseE E Blue, C-E Yu, T A Thornton, et al.
HGG Advances|July 17, 2023
Variants in <i>ACTC1</i> underlie distal arthrogryposis accompanied by congenital heart defectsJessica X Chong, Matthew Carter Childers, Colby T Marvin, et al.
Medrxiv : the Preprint Server for Health Sciences|March 22, 2023
Variants in <i>ACTC1</i> underlie distal arthrogryposis accompanied by congenital heart defectsJessica X Chong, Matthew Carter Childers, Colby T Marvin, et al.
American Journal of Human Genetics|January 1, 2013
Whole-genome analysis reveals that mutations in inositol polyphosphate phosphatase-like 1 cause opsismodysplasiaJennifer E Below, Dawn L Earl, Kathryn M Shively, et al.
American Journal of Human Genetics|May 11, 2015
Autosomal-Dominant Multiple Pterygium Syndrome Is Caused by Mutations in MYH3Jessica X Chong, Lindsay C Burrage, Anita E Beck, et al.
American Journal of Human Genetics|December 25, 2012
Mutations in ECEL1 cause distal arthrogryposis type 5DMargaret J McMillin, Jennifer E Below, Kathryn M Shively, et al.
American Journal of Human Genetics|April 2, 2013
Mutations in KCTD1 cause scalp-ear-nipple syndromeAlexander G Marneros, Anita E Beck, Emily H Turner, et al.
American Journal of Human Genetics|February 25, 2025
SeqFirst: Building equity access to a precise genetic diagnosis in critically ill newbornsTara L Wenger, Abbey Scott, Lukas Kruidenier, et al.
Pageof 10

Showing results (81-90 of 94) with videos related to

Sort By:
Pageof 10
Mammalian Genome : Official Journal of the International Mammalian Genome Society|August 17, 2013
Multiple mutant T alleles cause haploinsufficiency of Brachyury and short tails in Manx catsKati J Buckingham, Margaret J McMillin, Margaret M Brassil, et al.
Current Microbiology|January 10, 2003
Organization of carboxysome genes in the thiobacilliGordon C Cannon, Stefanie H Baker, Ferda Soyer, et al.
Genes, Brain, and Behavior|October 19, 2017
Variants regulating ZBTB4 are associated with age-at-onset of Alzheimer's diseaseE E Blue, C-E Yu, T A Thornton, et al.
HGG Advances|July 17, 2023
Variants in <i>ACTC1</i> underlie distal arthrogryposis accompanied by congenital heart defectsJessica X Chong, Matthew Carter Childers, Colby T Marvin, et al.
Medrxiv : the Preprint Server for Health Sciences|March 22, 2023
Variants in <i>ACTC1</i> underlie distal arthrogryposis accompanied by congenital heart defectsJessica X Chong, Matthew Carter Childers, Colby T Marvin, et al.
American Journal of Human Genetics|January 1, 2013
Whole-genome analysis reveals that mutations in inositol polyphosphate phosphatase-like 1 cause opsismodysplasiaJennifer E Below, Dawn L Earl, Kathryn M Shively, et al.
American Journal of Human Genetics|May 11, 2015
Autosomal-Dominant Multiple Pterygium Syndrome Is Caused by Mutations in MYH3Jessica X Chong, Lindsay C Burrage, Anita E Beck, et al.
American Journal of Human Genetics|December 25, 2012
Mutations in ECEL1 cause distal arthrogryposis type 5DMargaret J McMillin, Jennifer E Below, Kathryn M Shively, et al.
American Journal of Human Genetics|April 2, 2013
Mutations in KCTD1 cause scalp-ear-nipple syndromeAlexander G Marneros, Anita E Beck, Emily H Turner, et al.
American Journal of Human Genetics|February 25, 2025
SeqFirst: Building equity access to a precise genetic diagnosis in critically ill newbornsTara L Wenger, Abbey Scott, Lukas Kruidenier, et al.
Pageof 10