Showing results (151-160 of 157) with videos related to
Sort By:
Pageof 16
You have reached the last page of results.This site can display upto 157 results.
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.American Journal of Human Genetics|July 25, 2020
Mutations in MYLPF Cause a Novel Segmental Amyoplasia that Manifests as Distal ArthrogryposisJessica X Chong, Jared C Talbot, Emily M Teets, et al.Nature Cardiovascular Research|June 25, 2025
Maturation of human cardiac organoids enables complex disease modeling and drug discoveryMark W Pocock, Janice D Reid, Harley R Robinson, et al.American Journal of Human Genetics|February 17, 2015
De novo mutations in NALCN cause a syndrome characterized by congenital contractures of the limbs and face, hypotonia, and developmental delayJessica X Chong, Margaret J McMillin, Kathryn M Shively, et al.American Journal of Human Genetics|April 15, 2014
Mutations in PIEZO2 cause Gordon syndrome, Marden-Walker syndrome, and distal arthrogryposis type 5Margaret J McMillin, Anita E Beck, Jessica X Chong, et al.The Plant Cell|July 17, 2025
Designing a nitrogen-efficient cold-tolerant maize for modern agricultural systemsJonathan Odilón Ojeda-Rivera, Allison C Barnes, Elizabeth A Ainsworth, et al.Pageof 16