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Molecular studies of achondroplasia
Indian Journal of Orthopaedics, 05/14/09
Nahar R et al. - The study shows that confi rmation of clinical diagnosis of ACH by molecular genetic testing is essential to distinguish it from other skeletal dysplasias, to plan therapeutic options, and to offer genetic counseling. Management in patients confi rmed to have ACH, is briefl y discussed.
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