Jill Clayton-Smith

Publication Activity (10 Years)

Years Active: 2019-2021
Publications (10 Years): 3

Top Topics

Cross Sectional

Intellectual Disability

Top Venues

Orphanet journal of rare diseases

Clinical genetics

Clinical otolaryngology : official journal of ENT-UK ; official journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery

This page only lists publications with an associated author ORCID identifier.

Publications

Leslie Patricia Molina-Ramírez, Emma Mm Burkitt-Wright, Haroon Saeed, John Henry McDermott, Claire Kyle, Ronnie Wright, Christopher Campbell, Sanjeev S Bhaskar, Algy Taylor, Laura Dutton, Claire Forde, Kay Metcalfe, Audrey Smith, Jill Clayton-Smith, Sofia Douzgou Houge, Kate Chandler, Tracy A Briggs, Siddharth Banka, William G Newman, David Gokhale, Iain A Bruce, Graeme C M Black
The diagnostic utility of clinical exome sequencing in 60 patients with hearing loss disorders: A single-institution experience. Clinical otolaryngology : official journal of ENT-UK ; official journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery 46 (6) (2021)
Sofia Douzgou Houge, Myfanwy Rawson, Eulalia Baselga, Moise Danielpour, Laurence Faivre, Alon Kashanian, Kim M Keppler-Noreuil, Paul Kuentz, Grazia Maria Simonetta Mancini, Marie-Cecile Maniere, Victor Martínez-González, Victoria E Parker, Robert K Semple, Siddharth Srivastava, Pierre Vabres, Marie-Claire Y De Wit, John M Graham, Jill Clayton-Smith, Ghayda M Mirzaa, Barbara B Biesecker
A standard of care for individuals with PIK3CA-related disorders: An international expert consensus statement. Clinical genetics 101 (1) (2021)
Jill Clayton-Smith, Rebecca Bromley, John Dean, Hubert Journel, Sylvie Odent, Amanda Wood, Janet Williams, Verna Cuthbert, Latha Hackett, Neelo Aslam, Heli Malm, Gregory James, Lena Westbom, Ruth Day, Edmund Ladusans, Adam Jackson, Iain Bruce, Robert Walker, Sangeet Sidhu, Catrina Dyer, Jane Ashworth, Daniel Hindley, Gemma Arca Diaz, Myfanwy Rawson, Peter Turnpenny
Diagnosis and management of individuals with Fetal Valproate Spectrum Disorder; a consensus statement from the European Reference Network for Congenital Malformations and Intellectual Disability. Orphanet journal of rare diseases 14 (1) (2019)