R. Buckley, S. Schiff, and R. Schiff, Hematopoietic stem-cell transplantation for the treatment of severe combined immunodeficiency, N Engl J Med, vol.340, pp.508-524, 1999.

K. Chan and J. M. Puck, Development of a population-based screening for severe combined immunodeficiency, J Allergy Clin Immunol, vol.115, pp.391-399, 2005.

J. M. Puck and . Scid-newborn, Screening Working Group. Populationbased newborn screening for severe combined immunodeficiency: steps toward implementation, J Allergy Clin Immunol, vol.120, pp.760-768, 2007.

M. W. Baker, W. J. Grossman, R. H. Laessig, and G. L. , Development of a routine newborn screening protocol for severe combined immunodeficiency, J Allergy Clin Immunol, vol.124, pp.522-529, 2009.

J. M. Routes, W. J. Grossman, and J. Verbsky, Statewide newborn screening for severe T-cell lymphopenia, JAMA, vol.302, pp.2465-70, 2009.

J. L. Gerstel-thompson, J. F. Wilkey, and J. C. Baptiste, Highthroughput multiplexed T-cell-receptor excision circle quantitative PCR assay with internal controls for detection of severe combined immunodeficiency in population-based newborn screening, Clin Chem, vol.56, pp.1466-74, 2010.

A. M. Comeau, J. E. Hale, and S. Pai, Guidelines for implementation of population-based newborn screening for severe combined immunodeficiency, J Inherit Metab Dis, vol.33, pp.273-81, 2010.

J. Verbsky, M. W. Baker, and W. J. Grossman, Newborn screening for severe combined immunodeficiency; the Wisconsin experience, J Clin Immunol, vol.32, pp.82-90, 2012.

A. Kwan, J. A. Church, M. J. Cowan, R. Agarwal, N. Kapoor et al., Newborn screening for SCID and T cell lymphopenia in California: results of the first two years, J Allergy Clin Immunol, vol.132, pp.140-50, 2013.

A. Kwan, R. S. Abraham, R. Currier, A. Brower, K. Andruszewski et al., Newborn screening for severe combined immunodeficiency in 11 screening programs in the United States, JAMA, vol.312, p.729, 2014.

B. H. Vogel, V. Bonagura, G. A. Weinberg, M. Ballow, J. Isabelle et al., Newborn screening for SCID in New York state : experience from the first two years, J Clin Immunol, vol.34, pp.289-303, 2014.

J. King, J. F. Ludvigsson, and L. Hammarström, Newborn screening for primary immunodeficiency diseases: the past, the present and the future, Int J Neonatal Screen, vol.3, p.19, 2017.

C. Thomas, S. Mirallié, C. Pierres, C. Dert, M. C. Clément et al., Projet de mise en place du dépistage néonatal systématique des déficits immunitaires combinés sévères, Arch Pediatr, vol.22, pp.646-52, 2015.

M. Audrain, C. Thomas, and S. Mirallie, Evaluation of the T-cell receptor excision circle assay performances for severe combined immunodeficiency neonatal screening on Guthrie cards in a French single centre study, Clin Immunol, vol.150, pp.137-146, 2014.

M. Blom, I. Pico-knijnenburg, and M. Sijne-van-veen, An evaluation of the TREC assay with regard to the integration of SCID screening into the Dutch newborn screening program, Clin Immunol, vol.180, pp.106-116, 2017.

S. P. Adams, S. Rashid, T. Premachandra, K. Harvey, A. Ifederu et al., Screening of neonatal UK dried blood spots using a duplex TREC screening assay, J Clin Immunol, vol.34, pp.323-353, 2014.

Y. H. Chein, H. H. Yu, and N. C. Lee, Newborn screening for severe combined immunodeficiency in Taiwan, Int J Neonatal Screen, vol.3, p.16, 2017.

J. Van-der-spek, R. Groenwold, and M. Van-der-burg, TREC based newborn screening for severe combined immunodeficiency disease: a systematic review, J Clin Immunol, vol.35, pp.416-446, 2015.

E. Rechavi, A. Lev, T. Saraf-levy, A. Etzioni, S. Almashanu et al., Newborn screening for severe combined immunodeficiency in Israel, Int J Neonatal Screen, vol.3, p.13, 2017.