P. Cox

The transmembrane protein meckelin (MKS3) is mutated in Meckel-Gruber syndrome and the wpk rat

Ursula M. Smith, Mark Consugar, Louise Tee et al. · Nature Genetics · 2006 · 292 citations

Life Sciences, Genetics, Molecular Genetics +7

The Meckel–Gruber Syndrome proteins MKS1 and meckelin interact and are required for primary cilium formation

Helen R. Dawe, Ursula M. Smith, Andrew R. Cullinane et al. · Human Molecular Genetics · 2006 · 273 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Mutations in the Embryonal Subunit of the Acetylcholine Receptor (CHRNG) Cause Lethal and Escobar Variants of Multiple Pterygium Syndrome

Neil V. Morgan, Louise Brueton, P. Cox et al. · The American Journal of Human Genetics · 2006 · 165 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

Apoptosis in the Brains of Infants Suffering Intrauterine Cerebral Injury

A. David Edwards, Xuetian Yue, P. Cox et al. · Pediatric Research · 1997 · 125 citations

Life Sciences, Neurobiology, Neuroscience +12

A difficult conversation? The views and experiences of parents and professionals on the consent process for perinatal postmortem after stillbirth

E. Schmidt, P. Cox, Vicki Flenady et al. · BJOG An International Journal of Obstetrics & Gynaecology · 2012 · 123 citations

Medicine, Maternal Health, Obstetrics +13