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European Journal of Medical Genetics|March 25, 2009
Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individualsE K Bijlsma, A C J Gijsbers, J H M Schuurs-Hoeijmakers, et al.American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 16, 2013
Genotype and clinical care correlations in craniosynostosis: findings from a cohort of 630 Australian and New Zealand patientsT Roscioli, G Elakis, T C Cox, et al.Pageof 3