Daniel Guerrier
Rennes, France
Last Updated: 09/26/2026
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Found 9 publications
Correction: Variants in NR6A1 as a cause for congenital renal, vertebral and uterine anomalies.
Journal: Human genetics
Published: April 13, 2026
Genetic analyses using chromosomal microarray and exome sequencing in fetuses and women with Müllerian duct anomalies.
Journal: Journal of assisted reproduction and genetics
Published: April 29, 2025
Variants in NR6A1 as a cause for congenital renal, vertebral and uterine anomalies.
Journal: Human genetics
Published: December 21, 2024
Distinct requirements for PI3K isoforms p110α and p110δ for PIP3 synthesis in mouse oocytes and early embryos.
Journal: Development (Cambridge, England)
Published: September 17, 2024
Optimizing care for MRKH patients: From malformation screening to uterus transplantation eligibility.
Journal: Acta obstetricia et gynecologica Scandinavica
Published: June 25, 2024
High incidence of Mayer-Rokitansky-Küster-Hauser syndrome syndrome in third-generation DES women.
Journal: Therapie
Published: February 13, 2022
Involvement of ITIH5, a candidate gene for congenital uterovaginal aplasia (Mayer-Rokitansky-Küster-Hauser syndrome), in female genital tract development.
Journal: Gene expression
Published: January 01, 2012
The Mayer-Rokitansky-Küster-Hauser syndrome (congenital absence of uterus and vagina)--phenotypic manifestations and genetic approaches.
Journal: Journal of negative results in biomedicine
Published: July 01, 2005
Showing 1-9 of 9
Last Updated: 09/26/2026