Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Traffic (Copenhagen, Denmark)|September 14, 2001
Syntaxin 6: the promiscuous behaviour of a SNARE proteinF Wendler, S Tooze
European Journal of Cell Biology|March 1, 1984
Replication of coronavirus MHV-A59 in sac- cells: determination of the first site of budding of progeny virionsJ Tooze, S Tooze, G Warren
European Journal of Cell Biology|November 1, 1985
AtT20 pituitary tumour cells contain mouse mammary tumour virus and intracisternal A-type particles in addition to murine leukemia virusJ Tooze, S Tooze, H Haisma, et al.
Journal of Medical Genetics|December 21, 2022
Craniosynostosis, inner ear, and renal anomalies in a child with complete loss of <i>SPRY1</i> (sprouty homolog 1) functionRebecca S Tooze, Eduardo Calpena, Stephen R F Twigg, et al.
Genes|March 29, 2023
Review of Recurrently Mutated Genes in Craniosynostosis Supports Expansion of Diagnostic Gene PanelsRebecca S Tooze, Eduardo Calpena, Astrid Weber, et al.
European Journal of Human Genetics : EJHG|March 3, 2025
BCL11B-related disease: a single phenotypic entity?J Heather Vedovato-Dos-Santos, Rebecca S Tooze, Sivagamy Sithambaram, et al.
European Journal of Human Genetics : EJHG|May 17, 2024
The phenotype of MEGF8-related Carpenter syndrome (CRPT2) is refined through the identification of eight new patientsLaura M Watts, Marta Bertoli, Tania Attie-Bitach, et al.
Journal of Medical Genetics|January 31, 2024
BTB domain mutations perturbing KCTD15 oligomerisation cause a distinctive frontonasal dysplasia syndromeKerry A Miller, David A Cruz Walma, Daniel M Pinkas, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 25, 2021
Evaluating the performance of a clinical genome sequencing program for diagnosis of rare genetic disease, seen through the lens of craniosynostosisZerin Hyder, Eduardo Calpena, Yang Pei, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 8, 2023
Pathogenic variants in the paired-related homeobox 1 gene (PRRX1) cause craniosynostosis with incomplete penetranceRebecca S Tooze, Kerry A Miller, Sigrid M A Swagemakers, et al.
Pageof 2