Publications by authors named "S Kenwrick"

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Mutational Signature Analysis Reveals NTHL1 Deficiency to Cause a Multi-tumor Phenotype.
Judith E Grolleman, Richarda M de Voer, Fadwa A Elsayed, Maartje Nielsen, Robbert D A Weren, Sue Kenwrick

Cancer Cell· February 2019

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The role of genetic counsellors in genomic healthcare in the United Kingdom: a statement by the Association of Genetic Nurses and Counsellors.
Anna Middleton, Peter Marks, Anita Bruce, Liwsi K Protheroe-Davies, Cath King, Sue Kenwrick

Eur J Hum Genet· March 2017

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Mutations in ZIC2 in human holoprosencephaly: description of a novel ZIC2 specific phenotype and comprehensive analysis of 157 individuals.
Benjamin D Solomon, Felicitas Lacbawan, Sandra Mercier, Nancy J Clegg, Mauricio R Delgado, Sue Kenwrick

J Med Genet· August 2010

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A novel PCR approach for prenatal detection of the common NEMO rearrangement in incontinentia pigmenti.
Julie Steffann, Valérie Raclin, Asmae Smahi, Hayley Woffendin, Arnold Munnich, Sue J Kenwrick

Prenat Diagn· May 2004

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Pilot morpholino screen in Xenopus tropicalis identifies a novel gene involved in head development.
Sue Kenwrick, Enrique Amaya, Nancy Papalopulu

Dev Dyn· February 2004

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