Katrina Prescott

Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study

Jenny Lord, Dominic McMullan, Ruth Y. Eberhardt et al. · The Lancet · 2019 · 694 citations · Full text

<i>DICER1</i> syndrome: clarifying the diagnosis, clinical features and management implications of a pleiotropic tumour predisposition syndrome

I. Slade, Chiara Bacchelli, H. Davies et al. · Journal of Medical Genetics · 2011 · 361 citations · Full text

Genetic heterogeneity in Cornelia de Lange syndrome (CdLS) and CdLS-like phenotypes with observed and predicted levels of mosaicism

Morad Ansari, Gemma Poke, Quentin R. V. Ferry et al. · Journal of Medical Genetics · 2014 · 165 citations · Full text

Discriminating Power of Localized Three-Dimensional Facial Morphology

Peter Hammond, Tim J. Hutton, Judith Allanson et al. · The American Journal of Human Genetics · 2005 · 159 citations · Full text

Geometric Modeling, Facial Recognition System, Facial Animation +5

Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study

Lord J, McMullan DJ, Eberhardt RY et al. · Yearbook of pediatric endocrinology · 2019 · 155 citations

Genetics, Genetic Epidemiology, Diagnosis +22