The following pages link to Newborn screening
External toolsShowing 50 items.
View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Congenital iodine deficiency syndrome (links | edit)
- Genetic disorder (links | edit)
- Phenylketonuria (links | edit)
- Thyroid (links | edit)
- Adrenoleukodystrophy (links | edit)
- Neonatal heel prick (links | edit)
- Phenylalanine hydroxylase (links | edit)
- Severe combined immunodeficiency (links | edit)
- White ribbon (links | edit)
- Genetic testing (links | edit)
- Birth defect (links | edit)
- Congenital hypothyroidism (links | edit)
- Lucille Roybal-Allard (links | edit)
- Mike Simpson (links | edit)
- Congenital adrenal hyperplasia (links | edit)
- Galactosemia (links | edit)
- NBS (links | edit)
- Methylmalonic acidemias (links | edit)
- Medium-chain acyl-coenzyme A dehydrogenase deficiency (links | edit)
- Adenosine deaminase deficiency (links | edit)
- Prenatal testing (links | edit)
- Tandem mass spectrometry (links | edit)
- Congenital adrenal hyperplasia due to 21-hydroxylase deficiency (links | edit)
- Gas chromatography–mass spectrometry (links | edit)
- March of Dimes (links | edit)
- Muscular Dystrophy Association (links | edit)
- Glycogen storage disease type II (links | edit)
- Inborn errors of metabolism (links | edit)
- Krabbe disease (links | edit)
- Index of genetics articles (links | edit)
- Glycogen storage disease type I (links | edit)
- 3-Hydroxy-3-methylglutaryl-CoA lyase deficiency (links | edit)
- Systemic primary carnitine deficiency (links | edit)
- Michael H. Gelb (links | edit)
- Glutaric aciduria type 1 (links | edit)
- Clinical Laboratory Improvement Amendments (links | edit)
- Biotinidase deficiency (links | edit)
- Screening (medicine) (links | edit)
- Medical genetics (links | edit)
- 2,4 Dienoyl-CoA reductase deficiency (links | edit)
- 3-Methylcrotonyl-CoA carboxylase deficiency (links | edit)
- William Nyhan (links | edit)
- 2-Methylbutyryl-CoA dehydrogenase deficiency (links | edit)
- Neonatal screening (redirect page) (links | edit)
- List of biochemists (links | edit)
- List of MeSH codes (E05) (links | edit)
- List of MeSH codes (E01) (links | edit)
- List of MeSH codes (G03) (links | edit)
- List of MeSH codes (N05) (links | edit)
- List of MeSH codes (N02) (links | edit)
- Bio-MEMS (links | edit)
- Louis Isaac Woolf (links | edit)
- User:Poonwil1/BMDE501 Assignment (links | edit)
- User:Brainist/MeSH articles (links | edit)
- Spinal muscular atrophy (links | edit)
- Robert Guthrie (microbiologist) (links | edit)
- Maroteaux–Lamy syndrome (links | edit)
- Predictive medicine (transclusion) (links | edit)
- Public health genomics (links | edit)
- Galactose-1-phosphate uridylyltransferase deficiency (links | edit)