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ArticleMolecular syndromology2019

Extending the Phenotype and Identification of a Novel Candidate Gene for Immunodeficiency in 5q11 Microdeletion Syndrome.

Veronica Arora et al.PubMed ↗Full text ↗Publisher ↗

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1 paper cites it

2019
2020
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Full record →Abstract, authors, funding and every citing paper · PMID 30800048