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Genetic genealogy / Newborn screening / Maple syrup urine disease / Phenylketonuria / Methylmalonic acidemia / Propionic acidemia / Isovaleric acidemia / Galactosemia / Biotinidase deficiency / Health / Medicine / Rare diseases


Microsoft Word - 35 PS 621 et seq _2_.doc
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Document Date: 2012-07-10 11:10:50


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File Size: 19,28 KB

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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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