Mark Richards

Facioscapulohumeral muscular dystrophy (FSHD): an enigma unravelled?

N. Thomas, M. Upadhyaya, A. Belayew, 2011, Human Genetics.

Assessment of the potential pathogenicity of missense mutations identified in the GTPase‐activating protein (GAP)‐related domain of the neurofibromatosis type‐1 (NF1) gene

D. Cooper, M. Mort, M. Upadhyaya, 2012, Human mutation.

Microarray‐based copy number analysis of neurofibromatosis type‐1 (NF1)‐associated malignant peripheral nerve sheath tumors reveals a role for Rho–GTPase pathway genes in NF1 tumorigenesis

D. Cooper, N. Thomas, G. Spurlock, 2012, Human mutation.

Facioscapulohumeral muscular dystrophy (FSHD): an enigma unravelled?

N. Thomas, M. Upadhyaya, A. Belayew, 2012, Human Genetics.