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Public Health Genomics|March 5, 2026
The Path to Screening US Newborns for Severe Combined Immunodeficiency, 1968-2018: A Narrative Review of a Successful Biomedical Research and Public Health PartnershipScott D Grosse, Robert F Vogt, Golriz K Yazdanpanah, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 3, 2013
Decision-making process for conditions nominated to the recommended uniform screening panel: statement of the US Department of Health and Human Services Secretary's Advisory Committee on Heritable Disorders in Newborns and ChildrenAlex R Kemper, Nancy S Green, Ned Calonge, et al.
International Journal of Neonatal Screening|June 5, 2018
Case Definitions for Conditions Identified by Newborn Screening Public Health SurveillanceMarci K Sontag, Deboshree Sarkar, Anne M Comeau, et al.
Pediatrics|January 8, 2014
Parental permission for pilot newborn screening research: guidelines from the NBSTRNJeffrey R Botkin, Michelle Huckaby Lewis, Michael S Watson, et al.
Blood|June 16, 2016
Modeling altered T-cell development with induced pluripotent stem cells from patients with RAG1-dependent immune deficienciesPatrick M Brauer, Itai M Pessach, Erik Clarke, et al.
Frontiers in Pediatrics|April 27, 2019
Two Unique Cases of X-linked SCID: A Diagnostic Challenge in the Era of Newborn ScreeningPooja Purswani, Cristina Adelia Meehan, Hye Sun Kuehn, et al.
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