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Molecular and Cellular Biochemistry|May 17, 2014
Investigation into the potential for hypoxic interior of neoplasms to enhance HSPA expression in gliomaGlenda M Beaman, David A Phoenix, Sarah R Dennison, et al.Genes|August 27, 2021
The Genomic Architecture of Bladder Exstrophy Epispadias ComplexGlenda M Beaman, Raimondo M Cervellione, David Keene, et al.European Journal of Medical Genetics|September 16, 2018
Clinical and genetic heterogeneity in Melkersson-Rosenthal SyndromeYang Pei, Glenda M Beaman, David Mansfield, et al.The Pharmacogenomics Journal|August 9, 2024
Understanding general practitioner and pharmacist preferences for pharmacogenetic testing in primary care: a discrete choice experimentJohn H McDermott, Videha Sharma, Glenda M Beaman, et al.American Journal of Medical Genetics. Part A|January 11, 2019
22q11.2 duplications in a UK cohort with bladder exstrophy-epispadias complexGlenda M Beaman, Adrian S Woolf, Raimondo M Cervellione, et al.Clinical Genetics|October 29, 2021
Expanding the genotypic spectrum of TXNL4A variants in Burn-McKeown syndromeKatherine A Wood, Jamie M Ellingford, Huw B Thomas, et al.Frontiers in Pediatrics|March 24, 2025
Case Report: Prolonged survival in Schinzel-Giedion syndrome featuring megaureter and <i>de novo SETBP1</i> mutationGlenda M Beaman, Benjamin W Jarvis, Anju Goyal, et al.Reproductive Biomedicine Online|September 9, 2021
Biallelic loss of function variants in STAG3 result in primary ovarian insufficiencyLeigh A M Demain, Eline Boetje, Jonathan J Edgerley, et al.Journal of Pediatric Urology|May 1, 2022
Narrowing the chromosome 22q11.2 locus duplicated in bladder exstrophy-epispadias complexGlenda M Beaman, Adrian S Woolf, Filipa M Lopes, et al.European Journal of Medical Genetics|June 15, 2020
Ligase IV syndrome can present with microcephaly and radial ray anomalies similar to Fanconi anaemia plus fatal kidney malformationsRajesh Madhu, Glenda M Beaman, Kate E Chandler, et al.Pageof 3