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Clinical Dysmorphology|May 8, 1998
Rapadilino syndrome--a non-Finnish caseS G Kant, M Baraitser, P J Milla, et al.Clinical Dysmorphology|April 1, 1997
Selective IgG2 subclass deficiency--a marker for the syndrome of pre/postnatal growth retardation, developmental delay, hypotrophy of distal extremities, dental anomalies and eczemaS B Ainsworth, M Baraitser, R F Mueller, et al.Journal of Medical Genetics|February 1, 1987
An oculocerebral hypopigmentation syndrome: a case report with clinical, histochemical, and ultrastructural findingsM A Patton, M Baraitser, A H Heagerty, et al.Parkinsonism & Related Disorders|November 21, 2016
Lower urinary tract symptoms in Parkinson's disease: Prevalence, aetiology and managementClaire McDonald, Kristian Winge, David J BurnAmerican Journal of Medical Genetics|August 1, 1992
VACTERL with hydrocephalus: one end of the Fanconi anemia spectrum of anomalies?M E Porteous, I Cross, J BurnJournal of Chemical Theory and Computation|February 9, 2023
Gaussian Process Regression Models for Predicting Atomic Energies and Multipole MomentsMatthew J Burn, Paul L A PopelierJournal of Computational Chemistry|September 27, 2022
Producing chemically accurate atomic Gaussian process regression models by active learning for molecular simulationMatthew J Burn, Paul L A PopelierArchives of Disease in Childhood|September 18, 1999
Behavioural phenotype of Cornelia de Lange syndromeT P Berney, M Ireland, J BurnThe Journal of Chemical Physics|August 11, 2020
Creating Gaussian process regression models for molecular simulations using adaptive samplingMatthew J Burn, Paul L A PopelierNeuropediatrics|August 1, 1990
Megalencephaly with dysmyelination, spasticity, ataxia, seizures and distinctive neurophysiological findings in two siblingsM G Harbord, A Harden, B Harding, et al.Pageof 60