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Genes|October 23, 2021
Mechanisms of Genome Instability in the Fragile X-Related DisordersBruce E Hayward, Karen Usdin
The Journal of Molecular Diagnostics : JMD|August 19, 2017
Improved Assays for AGG Interruptions in Fragile X Premutation CarriersBruce E Hayward, Karen Usdin
Methods in Molecular Biology (Clifton, N.J.)|March 23, 2019
Assays for Determining Repeat Number, Methylation Status, and AGG Interruptions in the Fragile X-Related DisordersBruce E Hayward, Karen Usdin
Human Genetics|September 4, 2017
Recent advances in assays for the fragile X-related disordersBruce E Hayward, Daman Kumari, Karen Usdin
Nucleic Acids Research|July 4, 2020
A point mutation in the nuclease domain of MLH3 eliminates repeat expansions in a mouse stem cell model of the Fragile X-related disordersBruce E Hayward, Peter J Steinbach, Karen Usdin
The Journal of Molecular Diagnostics : JMD|August 17, 2016
A Set of Assays for the Comprehensive Analysis of FMR1 Alleles in the Fragile X-Related DisordersBruce E Hayward, Yifan Zhou, Daman Kumari, et al.
Diabetes|August 28, 2003
Properties of normal and mutant recombinant human ketohexokinases and implications for the pathogenesis of essential fructosuriaAruna Asipu, Bruce E Hayward, John O'Reilly, et al.
Nature|April 5, 2002
A global disorder of imprinting in the human female germ lineHannah Judson, Bruce E Hayward, Eamonn Sheridan, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|July 10, 2012
Recurrent hydatidiform mole: detection of two novel mutations in the NLRP7 gene in two Egyptian familiesEbtesam M Abdalla, Bruce E Hayward, Ahmed Shamseddin, et al.
Human Molecular Genetics|January 15, 2014
Chromosome fragility and the abnormal replication of the FMR1 locus in fragile X syndromeDmitry Yudkin, Bruce E Hayward, Mirit I Aladjem, et al.
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