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401	European Commission DGXI.E.3 (XURSHDQ3DFNDJLQJ:DVWH 0DQDJHPHQW6\VWHPV )LQDO5HSRUW )HEUXDU\ Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2014-10-30 09:05:55 Industrial design Industrial engineering Packaging and labeling Retailing Technology Green Dot Recycling Plastic recycling PET bottle recycling Waste management Sustainability Environment
402	Newborn Screening in Canada Status Report – Page 1 of 3 – updated November 8, 2013 ¹Follows format used by the U.S. National Newborn Screening & Genetics Resource Center A dot "" indicates that universal screenin Add to Reading List Source URL: www.raredisorders.ca Language: English - Date: 2013-11-18 10:15:10 Newborn screening Methylmalonic acidemia Propionic acidemia Isovaleric acidemia Glutaric aciduria type 1 Medical genetics Thiolase Carnitine Malonyl-CoA decarboxylase deficiency Health Rare diseases Medicine
403	European Commission DGXI.E.3 (XURSHDQ3DFNDJLQJ:DVWH 0DQDJHPHQW6\VWHPV 0DLQ5HSRUW )LQDO5HSRUW Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2014-10-30 09:05:57 Industrial design Industrial engineering Packaging and labeling Retailing Technology Waste Green Dot Reuse Plastics materials in India Waste management Sustainability Recycling
404	Newborn Screening in C anada Status Report ± Page 1 of 3 - updated Dec. 15, 2009 ¹Follows format used by the U.S. National Newborn Screening & Genetics Resource Center A dot "z" indicates that universal screening for t Add to Reading List Source URL: www.raredisorders.ca Language: English - Date: 2010-01-29 12:16:11 Coenzymes Metabolism Biology Newborn screening Propionic acidemia Carnitine Methylmalonic acidemia Glutaric aciduria type 1 Isovaleric acidemia Health Rare diseases Chemistry
405	Newborn Screening in Canada Status Report – Page 1 of 3 – updated June 21, 2013 ¹Follows format used by the U.S. National Newborn Screening & Genetics Resource Center A dot "" indicates that universal screening f Add to Reading List Source URL: www.raredisorders.ca Language: English - Date: 2013-06-27 10:49:23 Newborn screening Methylmalonic acidemia Propionic acidemia Isovaleric acidemia Glutaric aciduria type 1 Medical genetics Thiolase Carnitine Malonyl-CoA decarboxylase deficiency Health Rare diseases Medicine
406	Newborn Screening in Canada Status Report – Page 1 of 3 - updated Jan. 13, 2012 ¹Follows format used by the U.S. National Newborn Screening & Genetics Resource Center A dot "" indicates that universal screening for Add to Reading List Source URL: raredisorders.ca Language: English - Date: 2012-01-17 10:47:50 Chemistry Coenzymes Metabolism Epidemiology Newborn screening Pediatrics Propionic acidemia Methylmalonic acidemia Isovaleric acidemia Health Rare diseases Medicine
407	Newborn Screening in Canada Status Report – Page 1 of 3 – updated April 18, 2012 ¹Follows format used by the U.S. National Newborn Screening & Genetics Resource Center A dot "" indicates that universal screening Add to Reading List Source URL: raredisorders.ca Language: English - Date: 2012-04-20 11:01:56 Chemistry Newborn screening Propionic acidemia Methylmalonic acidemia Isovaleric acidemia Glutaric aciduria type 1 Thiolase Malonyl-CoA Carnitine palmitoyltransferase I Health Rare diseases Medicine
408	Newborn Screening in Canada Status Report – Page 1 of 3 - updated Nov. 11, 2010 ¹Follows format used by the U.S. National Newborn Screening & Genetics Resource Center A dot "" indicates that universal screening for Add to Reading List Source URL: www.raredisorders.ca Language: English - Date: 2010-11-11 13:21:56 Newborn screening Methylmalonic acidemia Propionic acidemia Isovaleric acidemia Hyperammonemia Glutaric aciduria type 1 Thiolase Maple syrup urine disease Methylmalonyl-CoA mutase Health Rare diseases Medicine
409	Newborn Screening in Canada Status Report – Page 1 of 3 – updated May 5, 2012 ¹Follows format used by the U.S. National Newborn Screening & Genetics Resource Center A dot "" indicates that universal screening for Add to Reading List Source URL: raredisorders.ca Language: English - Date: 2012-05-07 10:53:44 Chemistry Newborn screening Propionic acidemia Methylmalonic acidemia Isovaleric acidemia Glutaric aciduria type 1 Thiolase Malonyl-CoA Carnitine palmitoyltransferase I Health Rare diseases Medicine
410	National Newborn Screening and Genetics Resource Center Page 1 of 3 - updated October 2, 2006 For consistency this report follows the format used by the U.S. National Newborn Screening & Genetics Resource Center Dot "z" Add to Reading List Source URL: www.raredisorders.ca Language: English - Date: 2009-06-26 12:21:25 Medical genetics Newborn screening Propionic acidemia Methylmalonic acidemia Isovaleric acidemia Glutaric aciduria type 1 Methylmalonyl-CoA mutase Methylmalonic acid Thiolase Health Rare diseases Genetic genealogy

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