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Caroline Gernay

3

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Six novel variants in the MKRN3 gene causing central precocious puberty: characteristics of ten patients and their affected relatives

2021
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ROHHAD(NET) Syndrome: Systematic review of the clinical timeline and recommendations for diagnosis and prognosis.

2020 The Journal of Clinical Endocrinology and Metabolism
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Acute pancreatitis as initial presentation for hereditary spherocytosis: A case report

2016
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