[Analysis of the clinical application of next-generation sequencing in the diagnosis of neonatal hereditary spherocytosis].

Published 03/14/2026

Research record: [Analysis of the clinical application of next-generation sequencing in the diagnosis of neonatal hereditary spherocytosis].

Published in Zhonghua Er Ke Za Zhi; first publication date 2026-03-14. PMID 41834204.

This literature update records publication metadata from Europe PMC. Consult the original publication for its methods, findings and limitations.

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Source

Compiled from public manufacturer materials and regulatory sources. Not independently verified and not reviewed by a named clinician.

Published

2026-03-14

Updated

2026-10-20

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professional use

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