Showing results (441-450 of 860) with videos related to
Sort By:
Pageof 86
Journal of Neurological Surgery. Part B, Skull Base|January 18, 2014
Forces Applied at the Skull Base during Transnasal Endoscopic Transsphenoidal Pituitary Tumor ExcisionJames R Bekeny, Philip J Swaney, Robert J Webster, et al.ACS Omega|February 6, 2023
Simultaneous N-Deglycosylation and Digestion of Complex Samples on S-Traps Enables Efficient Glycosite Hypothesis GenerationChristine M DeRosa, Simon D Weaver, Chien-Wei Wang, et al.Journal of Agricultural and Food Chemistry|June 18, 2009
Impact of assay conditions on activity estimate and kinetics comparison of Aspergillus niger PhyA and Escherichia coli AppA2 phytasesJeremy D Weaver, Abul H J Ullah, Kandan Sethumadhavan, et al.Angiology|June 1, 1978
Tetralogy of Fallot associated with uncommon lesionsM D Weaver, J T Chen, D C Jackson, et al.The Journal of Clinical Investigation|April 1, 1984
A mutation that causes lability of the androgen receptor under conditions that normally promote transformation to the DNA-binding stateW J Kovacs, J E Griffin, D D Weaver, et al.American Journal of Medical Genetics. Part A|December 15, 2018
The progression of Wiedemann-Steiner syndrome in adulthood and two novel variants in the KMT2A geneHailey R Feldman, Stephen R Dlouhy, Melissa D Lah, et al.American Journal of Medical Genetics. Part A|April 14, 2007
On the spectrum of limb-body wall complex, exstrophy of the cloaca, and urorectal septum malformation sequenceCristin A Heyroth-Griffis, David D Weaver, Philip Faught, et al.Scientific Reports|May 19, 2025
Snooze alarm use in a global population of smartphone usersRebecca Robbins, Daniel Sääf, Matthew D Weaver, et al.Genetic Testing and Molecular Biomarkers|April 18, 2025
Uncovering a Diagnosis Through Reanalysis of UBA2 Variants in a Patient with Syndactyly, Polydactyly, and Aplasia Cutis Congenita: A Short Report and a Review of the LiteratureKhurram Liaqat, Kimberly Felipe, Kayla Treat, et al.Clinical Genetics|August 1, 1988
Neural tube defects and omphalocele in trisomy 18C A Moore, J P Harmon, L M Padilla, et al.Pageof 86