Guidelines for newborn screening of primary immunodeficiency diseases
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Hematology
Reference26 articles.
1. Journal Info Home About the Journal Editorial Board Archive Research Topics View Some Authors Review Guidelines Subscribe to Alerts Search Article Type Publication Date ...... Go Author Info Why Submit? Fees Article Types Author Guidelines Submission Checklist Contact Editorial Office Submit Manuscript Review ARTICLE Abstract Full Text PDF 0 Write a Comment Primary immunodeficiency diseases: an update on the classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency
2. Genetics of SCID
3. Neonatal diagnosis of severe combined immunodeficiency leads to significantly improved survival outcome: the case for newborn screening
4. Familial hemophagocytic lymphohistiocytosis type 3 (FHL3) caused by deep intronic mutation and inversion in UNC13D
5. Neonatal screening for severe primary immunodeficiency diseases using high-throughput triplex real-time PCR
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5. Neonatal Lymphopenia Screening Is Important For Early Diagnosis of Severe Combined Immunodeficiency;American Journal of Perinatology;2021-06-11
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