Mary J Gray

发表

Mutations in PYCR1 cause cutis laxa with progeroid features

Peter Nürnberg, Stefan Mundlos, Barry Merriman, 2009, Nature Genetics.

Serpentine fibula polycystic kidney syndrome is part of the phenotypic spectrum of Hajdu–Cheney syndrome

S. Robertson, M. Simpson, M. Irving, 2011, European Journal of Human Genetics.

Mutations in genes encoding the cadherin receptor-ligand pair DCHS1 and FAT4 disrupt cerebral cortical development

Sahar Mansour, Tim Morgan, Magdalena Götz, 2013, Nature Genetics.

A new acro-osteolysis syndrome caused by duplications including PTHLH

Paul Wordsworth, Tim Morgan, Paul Wordsworth, 2014, Journal of Human Genetics.