One-Year Evaluation of a Neonatal Screening Program for Cystic Fibrosis in Switzerland
Corina S. Rueegg(Oslo University Hospital), Juerg Barben(University of Zurich), Toni Torresani(University Children's Hospital Zurich), Claudia E. Kuehni(University of Bern), Sabina Gallati(University Children’s Hospital Bern), Matthias R. Baumgartner(University Children's Hospital Zurich)
Cited by 29
Related Papers
Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes
|New England Journal of Medicine|2008|811
Proposed guidelines for the diagnosis and management of methylmalonic and propionic acidemia
|Orphanet Journal of Rare Diseases|2014|713
European Society for Paediatric Endocrinology Consensus Guidelines on Screening, Diagnosis, and Management of Congenital Hypothyroidism
|The Journal of Clinical Endocrinology & Metabolism|2014|569
Vitamin B<sub>12</sub>, folate, and the methionine remethylation cycle—biochemistry, pathways, and regulation
|Journal of Inherited Metabolic Disease|2019|434