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Your Article Summary

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Carlsson G et al. - The authors describe a patient with a compound heterozygous HAX1 mutation consisting of a nonsense mutation and a frame-shift mutation resulting in a premature stop codon. The patient has a history of neutropenia and a propensity for infections, but has shown no signs of neurodevelopmental abnormalities.

Today in HemeOnc Emergencies...keeping you current

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Today in Pediatric Emergencies...keeping you current

Shock in the Critically Ill Neonate
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Observations on Increased Accidental Asphyxia Deaths in Infancy While Cosleeping in the State of Maryland
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Prospective analysis of a new minimally invasive technique for paediatric Gartland type III supracondylar fracture of the humerus
Injury, 11/25/09

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