Identification of 22q11.2 deletion syndrome via newborn screening for severe combined immunodeficiency. Two years' experience in Catalonia (Spain)
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| Description | scientific article published on 30 October 2019 |
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author: Ana Argudo-Ramírez Roger Colobran Andrea Martin-Nalda Mónica Martínez-Gallo Jacques G Rivière |
| Publication date | October 30, 2019 |
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