T-Cell Lymphopenia Detected by Newborn Screening in Two Siblings with an Xq13.1 Duplication

Newborn screening for severe combined immunodeficiency has proven successful in identifying infants with T-cell deficiencies before they become severely ill. Additionally, the newborn screen can detect subtle early phenotypes that may become severe later in life. We present the case of siblings with...

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Autores principales: Xavier Rios (Autor), Ivan K. Chinn (Autor), Jordan S. Orange (Autor), Celine I. Hanson (Autor), Nicholas L. Rider (Autor)
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Publicado: Frontiers Media S.A., 2017-07-01T00:00:00Z.
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