Sophie Dahoun
Geneve, GE, Switzerland
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 14 publications
A young girl with partial chromosome 15q11.2 microduplication: a case report in Cameroon.
Journal: BMC pediatrics
Published: December 19, 2025
Clinical, biochemical, and biomolecular aspects of congenital adrenal hyperplasia in a group of Cameroonian children and adolescents.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: November 19, 2021
Observational study of disorders of sex development in Yaounde, Cameroon.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: October 03, 2019
Feminizing genitoplasty for prepubertal children and teenagers female
Journal: Progres en urologie : journal de l'Association francaise d'urologie et de la Societe francaise d'urologie
Published: June 26, 2019
MECP2 duplication syndrome in a patient from Cameroon.
Journal: American journal of medical genetics. Part A
Published: May 22, 2019
Mixed gonadal dysgenesis in Yaoundé: A preliminary experience about three cases.
Journal: African journal of paediatric surgery : AJPS
Published: August 10, 2016
Laparoscopic-assisted vaginal pull-through: A new approach for congenital adrenal hyperplasia patients with high urogenital sinus.
Journal: African journal of paediatric surgery : AJPS
Published: November 28, 2015
Modelling and rescuing neurodevelopmental defect of Down syndrome using induced pluripotent stem cells from monozygotic twins discordant for trisomy 21.
Journal: EMBO molecular medicine
Published: December 31, 2013
Complex rearrangement of the exon 6 genomic region among Opitz G/BBB Syndrome MID1 alterations.
Journal: European journal of medical genetics
Published: February 13, 2013
Enhanced maternal origin of the 22q11.2 deletion in velocardiofacial and DiGeorge syndromes.
Journal: American journal of human genetics
Published: October 02, 2012
Last Updated: 09/26/2026