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	1.	Maternal isodisomy of the telomeric end of chromosome 2 is responsible for a case of primary hyperoxaluria type 1. [electronic resource] by Chevalier-Porst, Françoise Rolland, Marie-Odile Cochat, Pierre Bozon, Dominique Producer: 20050418 In: American journal of medical genetics. Part A vol. 132A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Are p.I148T, p.R74W and p.D1270N cystic fibrosis causing mutations? [electronic resource] by Claustres, Mireille Altiéri, Jean-Pierre Guittard, Caroline Templin, Carine Chevalier-Porst, Françoise Des Georges, Marie Producer: 20040816 In: BMC medical genetics vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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