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dnah11 protein human
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Primary ciliary dyskinesia associated with a novel DNAH11 genetic variant: a case report].
Investigation of the genetic and clinical features of laterality disorders in prenatal diagnosis: di…
Whole genome sequencing enhances molecular diagnosis of primary ciliary dyskinesia.
A Deep Intronic, Pathogenic Variant in DNAH11 Causes Primary Ciliary Dyskinesia.
Practical guide for the diagnosis and management of primary ciliary dyskinesia.
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