M. Redman

Biallelic PRMT7 pathogenic variants are associated with a recognizable syndromic neurodevelopmental disorder with short stature, obesity, and craniofacial and digital abnormalities

A. V. Vulto-van Silfhout, D. Baralle, P. Striano, 2022, Genetics in medicine : official journal of the American College of Medical Genetics.

Expanding SPTAN1 monoallelic variant associated disorders: From epileptic encephalopathy to pure spastic paraplegia and ataxia

A. Need, C. Tregidgo, J. Clayton-Smith, 2022, Genetics in medicine : official journal of the American College of Medical Genetics.

The ef fi cacy and safety of probiotics in people with cancer: a systematic review

R. Phillips, M. G. Redman, E. Ward, 2014 .

Rough endoplasmic reticulum expansion: a consistent finding in a patient cohort with vascular Ehlers-Danlos Syndrome and Osteogenesis Imperfecta

B. Wagner, D. Baker, Diana S. Johnson, 2021, Ultrastructural pathology.

Ancestry, race and ethnicity: the role and relevance of language in clinical genetics practice

M. Redman, Anneke Lucassen, R. Horton, 2023, Journal of medical genetics.