Identification of 22q11.2 deletion syndrome via newborn...

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Molecular Genetics & Genomic Medicine 2019 / 10

Identification of 22q11.2 deletion syndrome via newborn screening for severe combined immunodeficiency. Two years’ experience in Catalonia (Spain)

Martin‐Nalda, Andrea, Cueto‐González, Anna M., Argudo‐Ramírez, Ana, Marin‐Soria, Jose L., Martinez‐Gallo, Monica, Colobran, Roger, Plaja, Albert, Castells, Neus, Riviere, Jacques, Tizzano, Eduardo F.,
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Language:
english
Journal:
Molecular Genetics & Genomic Medicine
DOI:
10.1002/mgg3.1016
Date:
October, 2019
File:
PDF, 463 KB
english, 2019
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