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Journal of Medical Genetics|December 24, 1998
Locus heterogeneity in autosomal dominant congenital external ophthalmoplegia (CFEOM)G C Black, R Perveen, E Hatchwell, et al.
Ophthalmic Genetics|September 4, 2008
Bardet-biedl syndrome: an atypical phenotype in brothers with a proven BBS1 mutationPaul S Cannon, Jill Clayton-Smith, Philip L Beales, et al.
Clinical Dysmorphology|May 11, 2010
Familial 3q29 microdeletion syndrome providing further evidence of involvement of the 3q29 region in bipolar disorderJill Clayton-Smith, Carol Giblin, Rupert A Smith, et al.
Neurotoxicology and Teratology|November 20, 2018
Intellectual functioning in clinically confirmed fetal valproate syndromeRebecca L Bromley, Gus A Baker, Jill Clayton-Smith, et al.
Disease Markers|June 6, 2008
Stem cell biomarkers in chronic myeloid leukemiaXiaoyan Jiang, Yun Zhao, Donna Forrest, et al.
American Journal of Medical Genetics|February 15, 1992
Recurrent Wiedemann-Beckwith syndrome with inversion of chromosome (11)(p11.2p15.5)A M Norman, A P Read, J Clayton-Smith, et al.
European Journal of Human Genetics : EJHG|July 11, 2013
Dysmorphology at a distance: results of a web-based diagnostic serviceS Douzgou, J Clayton-Smith, S Gardner, et al.
European Journal of Medical Genetics|June 26, 2021
The adaptive functioning profile of Pitt-Hopkins syndromeEffie Pearson, Alice Watkins, Chris Oliver, et al.
Cancers|August 26, 2023
ASSET: Auto-Segmentation of the Seventeen SEgments for Ventricular Tachycardia Ablation in Radiation TherapyEric Morris, Robert Chin, Trudy Wu, et al.
American Journal of Medical Genetics. Part A|May 17, 2011
A novel 800 kb microduplication of chromosome 16q22.1 resulting in learning disability and epilepsy may explain phenotypic variability in a family with 15q13 microdeletionSiddharth Banka, Gregory J Fitzgibbon, Lorraine Gaunt, et al.
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