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Genotype-phenotype relationships in Freeman-Sheldon syndrome.
Sandhoff disease in Argentina: high frequency of a splice site mutation in the HEXB gene and correlation between enzyme and DNA-based tests for heterozygote detection.
Prescription Fees
Continuation rates of two different-sized copper intrauterine devices among nulliparous women: Interim 12-month results of a single-blind, randomised, multicentre trial.
AMYLOID PRECURSOR IN ALZHEIMER DISEASE
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