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	21.	Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individuals. [electronic resource] by Bijlsma, E K Gijsbers, A C J Schuurs-Hoeijmakers, J H M van Haeringen, A Fransen van de Putte, D E Anderlid, B-M Lundin, J Lapunzina, P Pérez Jurado, L A Delle Chiaie, B Loeys, B Menten, B Oostra, A Verhelst, H Amor, D J Bruno, D L van Essen, A J Hordijk, R Sikkema-Raddatz, B Verbruggen, K T Jongmans, M C J Pfundt, R Reeser, H M Breuning, M H Ruivenkamp, C A L Producer: 20090901 In: European journal of medical genetics vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	22.	Genotype and clinical care correlations in craniosynostosis: findings from a cohort of 630 Australian and New Zealand patients. [electronic resource] by Roscioli, T Elakis, G Cox, T C Moon, D J Venselaar, H Turner, A M Le, T Hackett, E Haan, E Colley, A Mowat, D Worgan, L Kirk, E P Sachdev, R Thompson, E Gabbett, M McGaughran, J Gibson, K Gattas, M Freckmann, M-L Dixon, J Hoefsloot, L Field, M Hackett, A Kamien, B Edwards, M Adès, L C Collins, F A Wilson, M J Savarirayan, R Tan, T Y Amor, D J McGillivray, G White, S M Glass, I A David, D J Anderson, P J Gianoutsos, M Buckley, M F Producer: 20140528 In: American journal of medical genetics. Part C, Seminars in medical genetics vol. 163C Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)