Geoffroy Delplancq

8PUBLICATIONS
43CO-AUTHORS
Adolescent healthChild language acquisitionEpigenetics (incl. genome methylation and epigenomics)Social epidemiologyGene mapping
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Publications (8)

|Nov 28, 2025
Severe Neurodevelopmental Disorder due to Klinefelter Syndrome and CACNA1C Variant: A Case Report.

Imen El Kamel El Lebbi, Séverine Bacrot, Myrtille Spentchian

|Feb 13, 2025
Deciphering the genetic basis of developmental language disorder in children without intellectual disability, autism or apraxia of speech.

Clothilde Ormieres, Marion Lesieur-Sebellin, Karine Siquier-Pernet

|Feb 29, 2024
3q29 duplications: A cohort of 46 patients and a literature review.

Marie Massier, Martine Doco-Fenzy, Matthieu Egloff

|Feb 16, 2023
TELO2-related syndrome (You-Hoover-Fong syndrome): Description of 14 new affected individuals and review of the literature.

Daniah Albokhari, Amanda Barone Pritchard, Adelyn Beil

|Dec 08, 2021
The Largest Germline Heterozygous Deletion Encompassing Potocki-Shaffer and WAGR Syndromes Loci to Date: A Case Report.

Geoffroy Delplancq, Mohamed Abdelatif Boukebir, Daniel Amsallem

|Oct 31, 2020
New Insights into Potocki-Shaffer Syndrome: Report of Two Novel Cases and Literature Review.

Slavica Trajkova, Eleonora Di Gregorio, Giovanni Battista Ferrero

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