Publications by authors named "Debra D Jeandron"

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A novel homozygous Q334X mutation in the HSD3B2 gene causing classic 3β-hydroxysteroid dehydrogenase deficiency: an unexpected diagnosis after a positive newborn screen for 21-hydroxylase deficiency.
Debra D Jeandron, Taninee Sahakitrungruang

Horm Res Paediatr· November 2012

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Neonatal hyperparathyroidism with a heterozygous calcium-sensing receptor (CASR) R185Q mutation: clinical benefit from cinacalcet.
Christina M S Reh, Geoffrey N Hendy, David E C Cole, Debra D Jeandron

J Clin Endocrinol Metab· April 2011

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