Last Posted: Sep 14, 2019
- Strengthening Public Health Laboratories: Newborn Screening and Genetics – Hemoglobinopathies Project
CDC, 2019 - Newborn Screening for Severe Combined Immunodeficiency.
Taki Mohammed et al. Pediatric clinics of North America 2019 Oct 66(5) 913-923 - Therapeutic advances in SMA.
Ludolph Albert C et al. Current opinion in neurology 2019 Oct (5) 777-781 - At-home genetic testing in pediatrics.
Weissman Scott M et al. Current opinion in pediatrics 2019 Aug - Hematopoietic Stem Cell Transplantation in Primary Immunodeficiency Diseases: Current Status and Future Perspectives.
Castagnoli Riccardo et al. Frontiers in pediatrics 2019 7295 - Multicenter Evaluation of HemoTypeSC as a Point-of-Care Sickle Cell Disease Rapid Diagnostic Test for Newborns and Adults Across India.
Mukherjee Malay B et al. American journal of clinical pathology 2019 Aug - Phenylketonuria incidence in China between 2013 and 2017 based on data from the Chinese newborn screening information system: a descriptive study.
Xiang Liangcheng et al. BMJ open 2019 Aug 9(8) e031474 - Recent advances in screening and diagnosis of haemoglobinopathy.
Ghosh Kanjaksha et al. Expert review of hematology 2019 Aug - Screening and mutation analysis of hyperphenylalaninemia in newborns from Xiamen, China.
Wang Xudong et al. Clinica chimica acta; international journal of clinical chemistry 2019 Aug - We must now put in place an updated, comprehensive newborn screening program for deaf and hard-of-hearing infants.
Howell R Rodney et al. Genetics in medicine : official journal of the American College of Medical Genetics 2019 Aug
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