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	1.	Whole exome sequencing identifies RAI1 mutation in a morbidly obese child diagnosed with ROHHAD syndrome. [electronic resource] by Thaker, Vidhu V Esteves, Kristyn M Towne, Meghan C Brownstein, Catherine A James, Philip M Crowley, Laura Hirschhorn, Joel N Elsea, Sarah H Beggs, Alan H Picker, Jonathan Agrawal, Pankaj B Producer: 20150930 In: The Journal of clinical endocrinology and metabolism vol. 100 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	A compound heterozygous mutation in GPD1 causes hepatomegaly, steatohepatitis, and hypertriglyceridemia. [electronic resource] by Joshi, Mugdha Eagan, Jacqueline Desai, Nirav K Newton, Stephanie A Towne, Meghan C Marinakis, Nicholas S Esteves, Kristyn M De Ferranti, Sarah Bennett, Michael J McIntyre, Adam Beggs, Alan H Berry, Gerard T Agrawal, Pankaj B Producer: 20150611 In: European journal of human genetics : EJHG vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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