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ArticleInternational journal of molecular sciences2023

Unusual Trisomy X Phenotype Associated with a Concurrent Heterozygous 16p11.2 Deletion: Importance of an Integral Approach for Proper Diagnosis.

Ariadna González-Del Angel et al.PubMed ↗Full text ↗Publisher ↗

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1 paper cites it

2023
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Full record →Abstract, authors, funding and every citing paper · PMID 37834089