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	1.	Peters Plus syndrome is caused by mutations in B3GALTL, a putative glycosyltransferase. [electronic resource] by Lesnik Oberstein, Saskia A J Kriek, Marjolein White, Stefan J Kalf, Margot E Szuhai, Karoly den Dunnen, Johan T Breuning, Martijn H Hennekam, Raoul C M Producer: 20061019 In: American journal of human genetics vol. 79 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Successful long-term growth hormone therapy in a girl with haploinsufficiency of the insulin-like growth factor-I receptor due to a terminal 15q26.2->qter deletion detected by multiplex ligation probe amplification. [electronic resource] by Walenkamp, Marie J E de Muinck Keizer-Schrama, Sabine M P F de Mos, Marianne Kalf, Margot E van Duyvenvoorde, Hermine A Boot, Annemieke M Kant, Sarina G White, Stefan J Losekoot, Monique Den Dunnen, Johan T Karperien, Marcel Wit, Jan M Producer: 20080717 In: The Journal of clinical endocrinology and metabolism vol. 93 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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