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	1.	Prenatal testing for a novel EBP missense mutation causing X-linked dominant chondrodysplasia punctata. [electronic resource] by Tysoe, Carolyn Law, Caroline J Caswell, Richard Clayton, Peter Ellard, Sian Producer: 20081104 In: Prenatal diagnosis vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Molecular characterisation of patients with subtelomeric 22q abnormalities using chromosome specific array-based comparative genomic hybridisation. [electronic resource] by Koolen, David A Reardon, William Rosser, Elisabeth M Lacombe, Didier Hurst, Jane A Law, Caroline J Bongers, Ernie M H F van Ravenswaaij-Arts, Conny M Leisink, Martijn A R van Kessel, Ad Geurts Veltman, Joris A de Vries, Bert B A Producer: 20051027 In: European journal of human genetics : EJHG vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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