![Genetic genealogy / Pediatrics / Newborn screening / Methylmalonic acidemia / Neonatal heel prick / Galactosemia / Biotinidase deficiency / 2-Methylbutyryl-CoA dehydrogenase deficiency / Hyperammonemia / Health / Medicine / Rare diseases Genetic genealogy / Pediatrics / Newborn screening / Methylmalonic acidemia / Neonatal heel prick / Galactosemia / Biotinidase deficiency / 2-Methylbutyryl-CoA dehydrogenase deficiency / Hyperammonemia / Health / Medicine / Rare diseases](https://www.pdfsearch.io/img/f7e0d65fbcfa21ef156d4a908d94d8e2.jpg) Date: 2013-10-04 10:41:36Genetic genealogy Pediatrics Newborn screening Methylmalonic acidemia Neonatal heel prick Galactosemia Biotinidase deficiency 2-Methylbutyryl-CoA dehydrogenase deficiency Hyperammonemia Health Medicine Rare diseases | | Chapter 4 : Newborn Screening Almost every child born in the United States undergoes state-mandated newborn screening. For each state, a small blood sample (“heel stick”) is collected from each newborn within 48 houAdd to Reading ListSource URL: www.geneticalliance.orgDownload Document from Source Website File Size: 113,62 KBShare Document on Facebook
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