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Human Mutation|June 18, 2009
Deletions in the VPS13B (COH1) gene as a cause of Cohen syndromeI Balikova, A-E Lehesjoki, T J L de Ravel, et al.
Neurology|September 2, 2016
Cognition in school-age children exposed to levetiracetam, topiramate, or sodium valproateRebecca L Bromley, Rebecca Calderbank, Christopher P Cheyne, et al.
Genes|April 28, 2023
The Role of Genetic Testing in Children Requiring Surgery for Ectopia LentisMohammud Musleh, Adam Bull, Emma Linton, et al.
Investigative Ophthalmology & Visual Science|August 11, 2000
Phenotypic variability and asymmetry of Rieger syndrome associated with PITX2 mutationsR Perveen, I C Lloyd, J Clayton-Smith, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|July 12, 2008
Folate and clefts of the lip and palate--a U.K.-based case-control study: Part II: Biochemical and genetic analysisJ Little, M Gilmour, P A Mossey, et al.
Nature|December 8, 2009
Large, rare chromosomal deletions associated with severe early-onset obesityElena G Bochukova, Ni Huang, Julia Keogh, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|December 17, 2003
Unrelated umbilical cord blood transplantation in adult patientsGwynn D Long, Mary Laughlin, Bella Madan, et al.
Brain : a Journal of Neurology|January 13, 2011
Foetal antiepileptic drug exposure and verbal versus non-verbal abilities at three years of ageKimford J Meador, Gus A Baker, Nancy Browning, et al.
Epilepsy & Behavior : E&B|May 7, 2011
Relationship of child IQ to parental IQ and education in children with fetal antiepileptic drug exposureKimford J Meador, Gus A Baker, Nancy Browning, et al.
Clinical Colorectal Cancer|July 23, 2020
Usefulness of Restaging Pelvis Magnetic Resonance Imaging After Neoadjuvant Concurrent Chemoradiotherapy in Patients With Locally Advanced Rectal CancerYazan Fahmawi, Clayton Smith, Leander Grimm, et al.
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