Showing results (11-20 of 75) with videos related to

Sort By:
Pageof 8
ACS Applied Materials & Interfaces|May 28, 2025
Multimodal Characterization of Rodent Dental DevelopmentYuchen Jiang, Kaitlin A Katsura, Nir Z Badt, et al.
Biorxiv : the Preprint Server for Biology|February 27, 2026
Unique mineralization pattern revealed in TBCK syndrome mouse modelKaitlin A Katsura, Yuchen Jiang, Marius Didziokas, et al.
American Journal of Medical Genetics. Part A|November 14, 2017
Expanding the phenotypic spectrum of TP63-related disorders including the first set of monozygotic twinsTara Wenger, Dong Li, Margaret H Harr, et al.
Biorxiv : the Preprint Server for Biology|November 18, 2024
Multi-modal characterization of rodent tooth developmentYuchen Jiang, Kaitlin A Katsura, Nir Z Badt, et al.
American Journal of Medical Genetics. Part A|March 7, 2022
Exome and RNA-Seq analyses of an incomplete penetrance variant in USP9X in female-specific syndromic intellectual disabilityDong Li, Michael E March, Tiancheng Wang, et al.
Molecular Genetics & Genomic Medicine|April 24, 2026
Clinical and Neurodevelopmental Course in a Case of EFNB1-Related Craniofrontonasal Syndrome With Unrepaired CraniosynostosisDominique L Assing, Danielle E Jolly, Sarah Gluschitz, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 21, 2016
Phenotypic predictors and final diagnoses in patients referred for RASopathy testing by targeted next-generation sequencingElizabeth J Bhoj, Zhenming Yu, Qiaoning Guan, et al.
American Journal of Medical Genetics. Part A|January 7, 2023
Genomic sequencing in a cohort of individuals with fibular aplasia, tibial campomelia, and oligosyndactyly (FATCO) syndromeDena R Matalon, Elizabeth J Bhoj, Dong Li, et al.
American Journal of Medical Genetics. Part A|February 24, 2015
Beare-Stevenson syndrome: two new patients, including a novel finding of tracheal cartilaginous sleeveTara L Wenger, Elizabeth J Bhoj, Ralph F Wetmore, et al.
American Journal of Medical Genetics. Part A|June 26, 2015
Exome sequencing expands the mechanism of SOX5-associated intellectual disability: A case presentation with review of sox-related disordersAddie Nesbitt, Elizabeth J Bhoj, Kristin McDonald Gibson, et al.
Pageof 8