Eric Dahlen
Besancon, France
Last Updated: 09/26/2026
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Found 10 publications
Correction: Comprehensive analysis of CNOT3-related neurodevelopmental disorders: phenotypic and genotypic characterization.
Journal: European journal of human genetics : EJHG
Published: April 02, 2026
Characterization of CTNND2-related neurodevelopmental disease, phenotype-genotype spectrum and WNT dynamics in early neurogenesis.
Journal: Research square
Published: January 08, 2026
Comprehensive analysis of CNOT3-related neurodevelopmental disorders: phenotypic and genotypic characterization.
Journal: European journal of human genetics : EJHG
Published: June 23, 2024
Comprehensive analysis of CNOT3-related neurodevelopmental disorders: phenotypic and genotypic characterization.
Journal: European journal of human genetics : EJHG
Published: June 23, 2024
Correspondence on "The ClinGen Brain Malformation Variant Curation Expert Panel: Rules for somatic variants in AKT3, MTOR, PIK3CA, and PIK3R2" by Lai et al.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: May 15, 2024
Evidence for high breakpoint variability in 46, XX, SRY-positive testicular disorder and frequent ARSE deletion that may be associated with short stature.
Journal: Andrology
Published: May 04, 2022
Bifid nose as the sole manifestation of BNAR syndrome, a FREM1-related condition.
Journal: Clinical genetics
Published: June 12, 2020
Post-Essential Thrombocythemia Myelofibrosis and Multiple Isodicentric Y Chromosomes: A Unique Case among a Rare Association.
Journal: Cytogenetic and genome research
Published: December 20, 2019
Showing 1-10 of 10
Last Updated: 09/26/2026