Identification of 22q11.2 Deletion Syndrome via Newborn Screening for Severe Combined Immunodeficiency. | Profiles RNS

RCMI Coordinating Center (RCMI CC)

Identification of 22q11.2 Deletion Syndrome via Newborn Screening for Severe Combined Immunodeficiency.

Barry JC, Crowley TB, Jyonouchi S, Heimall J, Zackai EH, Sullivan KE, McDonald-McGinn DM. Identification of 22q11.2 Deletion Syndrome via Newborn Screening for Severe Combined Immunodeficiency. J Clin Immunol. 2017 Jul; 37(5):476-485.

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authors with profiles

Kathleen Sullivan, APRN, PMHCNS-BC

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