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You searched for: Author/Creator Bainbridge, Matthew N

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1. Combination of whole exome sequencing and animal modeling identifies TMPRSS9 as a candidate gene for autism spectrum disorder. (15th January 2020)

2. Molecular subtyping of tumors from patients with familial glioma. Issue 6 (10th October 2017)

3. Phenotypic Variability of Osteogenesis Imperfecta Type V Caused by an IFITM5 Mutation. (18th June 2013)

4. POT1 mutation spectrum in tumour types commonly diagnosed among POT1-associated hereditary cancer syndrome families. Issue 10 (14th January 2020)