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You searched for: Author/Creator Castells, Neus

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1. Chromosomal microarray analysis in fetuses with central nervous system anomalies: An 8‐year long observational study from a tertiary care university hospital. (30th September 2020)

2. Chromosomal microarray analysis in fetuses with central nervous system anomalies: An 8‐year long observational study from a tertiary care university hospital. (30th September 2020)

3. Identification of 22q11.2 deletion syndrome via newborn screening for severe combined immunodeficiency. Two years' experience in Catalonia (Spain). Issue 12 (30th October 2019)

4. ZDHHC15 as a candidate gene for autism spectrum disorder. Issue 4 (23rd December 2022)