![Genetic genealogy / Newborn screening / Maple syrup urine disease / Phenylketonuria / Methylmalonic acidemia / Propionic acidemia / Isovaleric acidemia / Galactosemia / Biotinidase deficiency / Health / Medicine / Rare diseases Genetic genealogy / Newborn screening / Maple syrup urine disease / Phenylketonuria / Methylmalonic acidemia / Propionic acidemia / Isovaleric acidemia / Galactosemia / Biotinidase deficiency / Health / Medicine / Rare diseases](https://www.pdfsearch.io/img/007707a20a88fb17f7bcef5e29e802ac.jpg)
| Document Date: 2012-07-10 11:10:50 Open Document File Size: 19,28 KBShare Result on Facebook
Company Pennsylvania Bulletin / acyl-CoA / / Holiday Commonwealth Day / / MedicalCondition hemoglobinopathies / lyase deficiency / Galactosemia / mental retardation / Trifunctional protein deficiency / Tyrosinemia / Congenital adrenal hyperplasia / Diseases / mutase deficiency / DISEASE / PKU / Primary congenital hypothyroidism / sickle-cell disease / acidemia/Isovalery-CoA dehydrogenase deficiency / Beta-ketothiolase deficiency / Phenylketonuria / Biotinidase deficiency / Multiple carboxylase deficiency / Cystic fibrosis / acidemia/Propionyl-CoA carboxylase deficiency / carboxylase deficiency / maple syrup urine disease / Congenital hypothyroidism / Hb S/C disease / genetic diseases / Citrullinemia / Hb S/Beta-thalassemia / Homocystinuria / / Organization Department of Health / Newborn Screening and Follow-up Technical Advisory Board / State Advisory Health Board / Follow-up Technical Advisory Board / / Position Hb / / PublishedMedium the Pennsylvania Bulletin / /
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