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Browsing publications by Dr Sally Lynch

Newcastle AuthorsTitleYearFull text
Dr Marta Bertoli
Dr Ana Topf
Dr Lizzie Harris
Dr Steven Laval
Dr Anna Sarkozy
et al.		A novel mutation in PIEZO2 in a family presenting with autosomal dominant myopathy, ptosis, external ophthalmoplegia and distal symphalangism2015
Dr Brian Wilson
Dr Simon Zwolinski
Dr Laura Yates
Dr Sally Lynch
Microdeletion 1p35.2: A recognizable facial phenotype with developmental delay2015
Dr Sally Lynch
Alison Ross
Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling2015
Dr Sally Lynch
Dr Miranda Splitt
Weaver Syndrome and EZH2 Mutations: Clarifying the Clinical Phenotype2013
Dr Sally Lynch
Professor Judith Goodship
Dr Michael Wright
Dr Richard Fisher
How genetically heterogeneous is Kabuki syndrome?: MLL2 testing in 116 patients, review and analyses of mutation and phenotypic spectrum2012
Dr Timothy Cheetham
Dr Jonathan Wyllie
Dr Sally Lynch
Dr Simon Zwolinski
Lynn Prescott
et al.		8p23.1 duplication syndrome; a novel genomic condition with unexpected complexity revealed by array CGH2008
Dr Sally Lynch
Adults with Down's sydrome: The prevalence of complications and health care in the community2007
Dr Ross Henderson
Michael Clarke
Dr Sally Lynch
Inherited PAX6, NF1 and OTX2 mutations in a child with microphthalmia and aniridia2007
Dr Sally Lynch
Sandra Lodge
Healthcare of adults with Down's syndrome: prevalence of complications and review of medical care in a community setting2005
Dr Andrea Myers
Dr Lesley Kay
Dr Sally Lynch
Dr David Walker
Recurrence risk for psoriasis and psoriatic arthritis within sibships2005
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