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artículu científicu espublizáu n'ochobre de 2019 наукова стаття, опублікована 30 жовтня 2019 im Oktober 2019 veröffentlichter wissenschaftlicher Artikel wetenschappelijk artikel scientific article published on 30 October 2019
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2019-10-30T00:00:00Z
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Albert Plaja Neus Castells Pere Soler-Palacin Anna M Cueto-González Eduardo F Tizzano Jose L Marin-Soria
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Identification of 22q11.2 deletion syndrome via newborn screening for severe combined immunodeficiency. Two years' experience in Catalonia (Spain) Identification of 22q11.2 deletion syndrome via newborn screening for severe combined immunodeficiency. Two years' experience in Catalonia (Spain)
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Identification of 22q11.2 deletion syndrome via newborn screening for severe combined immunodeficiency. Two years' experience in Catalonia (Spain) Identification of 22q11.2 deletion syndrome via newborn screening for severe combined immunodeficiency. Two years' experience in Catalonia (Spain)
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Identification of 22q11.2 deletion syndrome via newborn screening for severe combined immunodeficiency. Two years' experience in Catalonia (Spain) Identification of 22q11.2 deletion syndrome via newborn screening for severe combined immunodeficiency. Two years' experience in Catalonia (Spain)
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Identification of 22q11.2 deletion syndrome via newborn screening for severe combined immunodeficiency. Two years' experience in Catalonia (Spain)
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