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	1.	Mutations in HYAL1, a member of a tandemly distributed multigene family encoding disparate hyaluronidase activities, cause a newly described lysosomal disorder, mucopolysaccharidosis IX. [electronic resource] by Triggs-Raine, B Salo, T J Zhang, H Wicklow, B A Natowicz, M R Producer: 19990624 In: Proceedings of the National Academy of Sciences of the United States of America vol. 96 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Comparison of anthropometric measurements in children to predict metabolic syndrome in adolescence: analysis of prospective cohort data. [electronic resource] by Wicklow, B A Becker, A Chateau, D Palmer, K Kozyrskij, A Sellers, E A C Producer: 20160516 In: International journal of obesity (2005) vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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