Birth Defects & Child Health
Clinical utility gene card for: Prader-Willi Syndrome![External Web Site Icon External Web Site Icon](https://lh3.googleusercontent.com/blogger_img_proxy/AEn0k_tDi6j3k1p9CW3fwK58dJOPh4DhoUIQdEpD6QLKRpbGfeyOoCdYuNJ4Q3hIkmLykwG84cPR6CyxqinRxLL1zVRDPslVF8hxbk6iIx_2XaNoKxQ_Hl9wC8zI=s0-d)
Buiting K, et al. Eur J Hum Genet 2014 Apr
Buiting K, et al. Eur J Hum Genet 2014 Apr
National Institutes of Health (NIH) review of evidence in phenylalanine hydroxylase deficiency (phenylketonuria) and recommendations/guidelines for therapy from the American College of Medical Genetics (ACMG) and Genetics Metabolic Dietitians International (GMDI).![External Web Site Icon External Web Site Icon](https://lh3.googleusercontent.com/blogger_img_proxy/AEn0k_tDi6j3k1p9CW3fwK58dJOPh4DhoUIQdEpD6QLKRpbGfeyOoCdYuNJ4Q3hIkmLykwG84cPR6CyxqinRxLL1zVRDPslVF8hxbk6iIx_2XaNoKxQ_Hl9wC8zI=s0-d)
Greene CL, et al. Mol Genet Metab. 2014 Mar 25. pii: S1096-7192(14)00093-6.
Greene CL, et al. Mol Genet Metab. 2014 Mar 25. pii: S1096-7192(14)00093-6.
Phenylketonuria scientific review conference: State of the science and future research needs.![External Web Site Icon External Web Site Icon](https://lh3.googleusercontent.com/blogger_img_proxy/AEn0k_tDi6j3k1p9CW3fwK58dJOPh4DhoUIQdEpD6QLKRpbGfeyOoCdYuNJ4Q3hIkmLykwG84cPR6CyxqinRxLL1zVRDPslVF8hxbk6iIx_2XaNoKxQ_Hl9wC8zI=s0-d)
Camp KM, et al. Mol Genet Metab. 2014 Mar 6. pii: S1096-7192(14)00085-7.
Camp KM, et al. Mol Genet Metab. 2014 Mar 6. pii: S1096-7192(14)00085-7.
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