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Aplastic anemia; CD34; Cord blood stem cell transplantation; Peripheral blood stem cell transplantation
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Novel Pathogenic Variant (c.3178G>A) in the SMC1A Gene in a Family With Cornelia de Lange Syndrome Identified by Exome Sequencing
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A family with X-linked Cornelia de Lange syndrome due to a novel SMC1A missense mutation identified by multi-gene panel sequencing
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Successful difficult airway management using GlideScope video laryngoscope in a child with Cornelia de Lange Syndrome
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