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A 3D Clinical Face Phenotype Space of Genetic Syndromes Using a Triplet-Based Singular Geometric Autoencoder by Soha S. Mahdi, Eduarda Caldeira, Harold Matthews, Michiel Vanneste, Nele Nauwelaers, Meng Yuan, Giorgos Bouritsas, Gareth S. Baynam, Peter Hammond, Richard Spritz, Ophir D. Klein, Michael Bronstein, Benedikt Hallgrimsson, Hilde Peeters, Peter Claes
Published 2025-01-01Get full text
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Uncovering genomic causes of co-morbidity in epilepsy: gene-driven phenotypic characterization of rare microdeletions. by Dalia Kasperavičiūtė, Claudia B Catarino, Krishna Chinthapalli, Lisa M S Clayton, Maria Thom, Lillian Martinian, Hannah Cohen, Shazia Adalat, Detlef Bockenhauer, Simon A Pope, Nicholas Lench, Martin Koltzenburg, John S Duncan, Peter Hammond, Raoul C M Hennekam, John M Land, Sanjay M Sisodiya
Published 2011-01-01Get full text
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