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Proposal for a new risk model in myelodysplastic syndrome that accounts for events not considered in the original International Prog...
Human ATP-Binding Cassette Transporter 1 (ABC1): Genomic Organization and Identification of the Genetic Defect in the Original Tangi...
Association of HbA1c with prevalent cardiovascular disease in the original cohort of the Framingham Heart Study
An LRRK2 mutation as a cause for the parkinsonism in the original PARK8 family.
An additional unique candidate mutation (G2470A; M740I) in the original families with von Willebrand disease type 2 M Vicenza and th...
STAT3 mutation in the original patient with Job's syndrome.
Evidence of MEN-2 in the Original Description of Classic Pheochromocytoma
Genomic organization and identification of the genetic defect in the original Tangier disease kindred
Tracking of glycated hemoglobin in the original cohort of the Framingham Heart Study
Equipment adaptable to brewing coffee in the original sealed container
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