Baby Detect : Genomic Newborn Screening

Conditions:   Congenital Adrenal Hyperplasia;   Familial Hyperinsulinemic Hypoglycemia 1;   Phosphoglucomutase 1 Deficiency;   Maturity Onset Diabetes of the Young;   Cystic Fibrosis;   Hypophosphatasia, Infantile;   Congenital Hypothyroidism;   DAVID;   Pituitary Hormone Deficiency,  Combined;   Diamond Blackfan Anemia;   Wiskott-Aldrich Syndrome;   Fanconi Anemia;   Hemophilia A;   Hemophilia B;   Glucose 6 Phosphate Dehydrogenase Deficiency;   Alpha-Thalassemia;   Sickle Cell Disease;   Shwachman-Diamond Syndrome;   Alpha 1-Antitrypsin Deficiency;   I nflammatory Bowel Disease 25, Autosomal Recessive;   Wilson Disease;   Progressive Familial Intrahepatic Cholestasis;   Crigler-Najjar Syndrome;   DIAR4;   Familial Chylomicronemia;   Lysosomal Acid Lipase Deficiency;   Familial Hemophagocytic Lymphocytosis;   Griscelli Syndrome;   Chediak-Higashi Syndrome;   Severe Congenital Neutropenia;   SCID;   Chronic Granulomatous Disease;   Menkes Disease;   X-ALD;   Smith-Lemli-Opitz Syndrome;   Ataxia With Vitamin E Deficiency;   THMD5;   THMD4;   Thiamine-Responsive Megaloblastic Anemia;   Thiamine Metab olism Dysfunction Syndrome 2;   GOT2 DEFICIENCY;   Cerebral Folate Transport Deficiency;   Segawa Syndrome, Autosomal Recessive;   Congenital Myasthenic Syndrome;   Metachromatic Leukodystrophy;   Sepiapterin Reductase Deficiency;   Dopamine Beta Hydroxylase D...
Source: ClinicalTrials.gov - Category: Research Source Type: clinical trials