Last Posted: Nov 08, 2019
- All children to receive whole genome sequencing at birth
The Telegraph, November 7, 2019 - Ensuring the Life-Span Benefits of Newborn Screening.
Kemper Alex R et al. Pediatrics 2019 Nov - Cystic Fibrosis Diagnosis in Newborns, Children, and Adults.
Castellani Carlo et al. Seminars in respiratory and critical care medicine 2019 Nov - Cystic fibrosis newborn screening in Denmark: Experience from the first 2 years.
Skov Marianne et al. Pediatric pulmonology 2019 Nov - Identification of 22q11.2 deletion syndrome via newborn screening for severe combined immunodeficiency. Two years' experience in Catalonia (Spain).
Martin-Nalda Andrea et al. Molecular genetics & genomic medicine 2019 Oct e1016 - Newborn Screening for Inherited Metabolic Disorders: Early Identification and Long-Term Care for Patients in the Plain Community, Wisconsin, 2011-2017.
Held Patrice K et al. Public health reports (Washington, D.C. : 1974) 134(2_suppl) 58S-63S - [Newborn screening program and blood amino acid profiling in early neonates with citrin deficiency].
Tang C F et al. Zhonghua er ke za zhi = Chinese journal of pediatrics 2019 Oct 57(10) 797-801 - [Newborn screening of sickle cell disease and management of care.]
Allaf Bichr et al. La Revue du praticien 2019 Apr 69(4) 411-416 - 22q and two: 22q11.2 deletion syndrome and coexisting conditions.
Cohen Jennifer L et al. American journal of medical genetics. Part A 2018 176(10) 2203-2214 - Fourth Update on the Iranian National Registry of Primary Immunodeficiencies: Integration of Molecular Diagnosis.
Abolhassani Hassan et al. Journal of clinical immunology 2018 38(7) 816-832
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