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Publications by Rachel Reynaud

Mutations in the Maternally Imprinted Gene MKRN3 Are Common in Familial Central Precocious Puberty

European Journal of Endocrinology
MedicineEndocrinologyMetabolismDiabetes
2016English

Using Digital Droplet Polymerase Chain Reaction to Detect the Mosaic GNAS Mutations in Whole Blood DNA or Circulating Cell-Free DNA in Fibrous Dysplasia and McCune-Albright Syndrome

Journal of Pediatrics
Child HealthPediatricsPerinatology
2019English

SFE/SFEDP Adrenal Insufficiency French Consensus: Introduction and Handbook

Annales d'Endocrinologie
MedicineEndocrinologyMetabolismDiabetes
2018English

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