A. Murray

A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD

David Heckerman, Lorne Zinman, Joanne Wuu, 2011, Neuron.

Familial motor neurone disease with dementia: phenotypic variation and cerebellar pathology

P. Harper, J. Neal, T. Polvikoski, 2003, Journal of neurology, neurosurgery, and psychiatry.

Familial frontotemporal dementia with amyotrophic lateral sclerosis and a shared haplotype on chromosome 9p

D. Hernandez, A. Singleton, N. Williams, 2011, Journal of Neurology.

Eighth International workshop on the fragile X syndrome and X-linked mental retardation, August 16-22, 1997.

C. Gunter, C. Schwartz, W. Brown, 1999, American journal of medical genetics.

Developing a quality scoring system for epidemiological surveys of genetic disorders

A. Murray, J. Layzell, R. Newcombe, 2002, Clinical genetics.

A case of multiple cutaneous schwannomas; schwannomatosis or neurofibromatosis type 2?

D. Evans, P. Harper, J. Neal, 2006, Journal of Neurology, Neurosurgery & Psychiatry.

Typical 22q11.2 deletion syndrome appears to confer a reduced risk of schwannoma

W. Foulkes, L. Messiaen, D. Stevenson, 2021, Genetics in Medicine.

Down's syndrome with a familial D/D reciprocal translocation and a G/G chromosome.

H. B. Marsden, A. Murray, R. Mackay, 1966, Journal of medical genetics.