Your search returned 3 results.

Results
	1.	Familial congenital esophageal atresia. Personal case report and review of the literature. [electronic resource] by Van Staey, M De Bie, S Matton, M T De Roose, J Producer: 19840530 In: Human genetics vol. 66 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Dominant optic nerve atrophy with progressive hearing loss and chronic progressive external ophthalmoplegia (CPEO). [electronic resource] by Meire, F De Laey, J J de Bie, S van Staey, M Matton, M T Producer: 19851219 In: Ophthalmic paediatrics and genetics vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Ehlers-Danlos syndrome type I: a clinical and ultrastructural study of a family with reduced amounts of collagen type III. [electronic resource] by De Paepe, A Nicholls, A Narcisi, P De Keyser, F Quatacker, J Van Staey, M Matton, M Pope, F M Producer: 19871120 In: The British journal of dermatology vol. 117 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

Refine your search