Peter Farndon

Complications of the naevoid basal cell carcinoma syndrome: results of a population based study.

D. Gareth Evans, E J Ladusans, S. Rimmer et al. · Journal of Medical Genetics · 1993 · 594 citations · Full text

Ophthalmology, Many Potential Complications, Ear Molding +10

A Novel X-Linked Disorder of Immune Deficiency and Hypohidrotic Ectodermal Dysplasia Is Allelic to Incontinentia Pigmenti and Due to Mutations in IKK-gamma (NEMO)

Jonathan Zonana, Melissa E. Elder, Lynda C. Schneider et al. · The American Journal of Human Genetics · 2000 · 521 citations · Full text

Novel X-linked Disorder, Urology, Immune Deficiency +10

The fetal valproate syndrome

John H. DiLiberti, Peter Farndon, Nicholas R. Dennis et al. · American Journal of Medical Genetics · 1984 · 397 citations

Developmental Toxicology, Fetal Medicine, Pediatrics +13

Location of gene for Gorlin syndrome

Peter Farndon, Richard G. Del Mastro, M W Kilpatrick et al. · The Lancet · 1992 · 396 citations

Mendelian Disorder, Genetic Disorder, Genetics +7

A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene

Maria Bitner‐Glindzicz, Keith Lindley, Paul Rutland et al. · Nature Genetics · 2000 · 324 citations

Infantile Hyperinsulinism, Mendelian Disorder, Genetic Disorder +9