Browsing publications by Dr Paul Brennan

Newcastle AuthorsTitleYearFull text
Dr Jannath Ahmed
Dr Simon Zwolinski
Dr Paul Brennan
Dr Neil Rajan
A novel contiguous heterozygous deletion involving the desmoglein 2 and desmocollin 2 genes is associated with arrhythmogenic right ventricular cardiomyopathy2016
Dr Paul Brennan
SOS1 frameshift mutations cause pure mucosal neuroma syndrome, a clinical phenotype distinct from multiple endocrine neoplasia type 2B2016
Mark Brady
Dr Paul Brennan
Professor John Sayer
Diagnosing Fabry disease-delays and difficulties within discordant siblings2015
Dr Paul Brennan
Breast cancer risk in MEN1 – a cancer genetics perspective2014
Dr Paul Brennan
Case-finding in Fabry disease: experience from the North of England2014
Dr Paul Brennan
Dr Stephen Ball
Professor Thomas Lennard
Familial endocrine disease: genetics, clinical presentation and management2014
Dr Paul Brennan
Cancer family history triage: a key step in the decision to offer screening and genetic testing2013
Dr Paul Brennan
Dr Julia Cook
Dr Theresa Cole
Dr Stephen Ball
Dr Fiona MacDonald
et al.
Evaluation of SDHB, SDHD and VHL gene susceptibility testing in the assessment of individuals with non-syndromic phaeochromocytoma, paraganglioma and head and neck paraganglioma2013
Dr Brian Wilson
Dr Paul Brennan
Juvenile idiopathic arthritis, mitral valve proplapse and a familial variant involving the integrin-binding fragment of FBN12013
Dr Paul Brennan
Dr Andrew Carmichael
New mutation identified in adult onset erythropoeitic protoporphyria2013
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