Clemence Delcour
Paris, France
Last Updated: 09/26/2026
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Found 16 publications
Annotating rare variants: A challenge that has not been completely resolved.
Journal: Annales d'endocrinologie
Published: March 22, 2026
MKRN3 Variants in Central Precocious Puberty as an Example of the Complexity to Classify Missense Variants in Imprinted Genes as Pathogenic.
Journal: Hormone research in paediatrics
Published: August 05, 2025
Biallelic null RAB3GAP1 variants impair cortical development and autophagy in Warburg Micro syndrome: evidence from fetal brain tissue and patient fibroblasts.
Journal: Acta neuropathologica communications
Published: July 10, 2025
Uterine Venous Malformation as a Rare Cause of Prepubertal Vaginal Bleeding.
Journal: Pediatrics
Published: February 13, 2025
Endocrine management of transgender adolescents: Expert consensus of the french society of pediatric endocrinology and diabetology working group.
Journal: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie
Published: August 02, 2024
Genito-urinary Reconstruction in Female Children With Congenital Adrenal Hyperplasia: Favorable Surgical Outcomes can be Achieved by Contemporary Techniques and a Dedicated Multidisciplinary Management.
Journal: Journal of pediatric surgery
Published: January 02, 2024
Ovarian tissue cryopreservation for fertility preservation before hematopoietic stem cell transplantation in patients with sickle cell disease: safety, ovarian function follow-up, and results of ovarian tissue transplantation.
Journal: Journal of assisted reproduction and genetics
Published: November 23, 2023
Care for transgender children and adolescents
Journal: Medecine sciences : M/S
Published: November 30, 2022
Early formative objective structured clinical examinations for students in the pre-clinical years of medical education: A non-randomized controlled prospective pilot study.
Journal: PloS one
Published: August 18, 2022
Turner syndrome: French National Diagnosis and Care Protocol (NDCP; National Diagnosis and Care Protocol).
Journal: Orphanet journal of rare diseases
Published: February 28, 2022
Fetal and Neonatal Thyroid Dysfunction.
Journal: The Journal of clinical endocrinology and metabolism
Published: September 13, 2021
Estrogen Receptor α Inactivation in 2 Sisters: Different Phenotypic Severities for the Same Pathogenic Variant.
Journal: The Journal of clinical endocrinology and metabolism
Published: July 11, 2021
Last Updated: 09/26/2026