Identification of 22q11.2 Deletion Syndrome via Newborn Screening for Severe Combined Immunodeficiency
Author:
Funder
National Institutes of Health
National Institute of Mental Health
Publisher
Springer Science and Business Media LLC
Subject
Immunology,Immunology and Allergy
Link
http://link.springer.com/article/10.1007/s10875-017-0403-9/fulltext.html
Reference39 articles.
1. Rivers L, Gaspar HB. Severe combined immunodeficiency: recent developments and guidance on clinical management. Arch Dis Child. 2015;100:667–72.
2. Kwan A, Puck JM. History and current status of newborn screening for severe combined immunodeficiency. Semin Perinatol. 2015;39:194–205.
3. Chinn IK, Shearer WT. Severe combined immunodeficiency disorders. Immunol Allergy Clin N Am. 2015;35(4):671–94.
4. Pai SY, Logan BR, Griffith LM, Buckley RH, Parrott RE, Dvorak CC. Retrospective study of 240 patients with severe combined immunodeficiency transplanted from 2000-2009: a report from the primary immune deficiency treatment consortium of North America. Biol Blood Marrow Transplant. 2014;20(2S):S24–5.
5. Kwan A, Abraham RS, Currier R, Brower A, Andruszewski K, Abbott JK, et al. Newborn screening for SCID in 11 screening programs in the US. JAMA. 2014;312(7):729–38.
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3. Impact of high‐risk prenatal screening results for 22q11.2 deletion syndrome on obstetric and neonatal management: Secondary analysis from the SMART study;Prenatal Diagnosis;2023-12
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5. Chromosome 22q11.2 Deletion Syndrome: A Comprehensive Review of Molecular Genetics in the Context of Multidisciplinary Clinical Approach;International Journal of Molecular Sciences;2023-05-05
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