Incidence of Smith-Lemli-Opitz syndrome in Canada: Results of three-year population surveillance
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology and Child Health
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4. Mutations in the human sterol Δ7-reductase gene at 11q12-13 cause Smith-Lemli-Opitz syndrome;Wassif;Am J Hum Genet,1998
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