Clémence Jacquin

4PUBLICATIONS
12CO-AUTHORS
Foetal development and medicineEpigenetics (incl. genome methylation and epigenomics)Gene mappingDevelopmental genetics (incl. sex determination)
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Publications (4)

|Jul 15, 2026
Parental Decision-Making and Pregnancy Outcomes After Increased First-Trimester Nuchal Translucency: A 12-Year Cohort.

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

Marie Massier, Martine Doco-Fenzy, Matthieu Egloff

|Nov 12, 2022
1p36 deletion syndrome: Review and mapping with further characterization of the phenotype, a new cohort of 86 patients.

Clémence Jacquin, Emilie Landais, Céline Poirsier

|Oct 05, 2022
Clinical and genomic delineation of the new proximal 19p13.3 microduplication syndrome.

Guillaume Jouret, Matthieu Egloff, Emilie Landais

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Frequent Collaborators

2 joint publications

Guillaume Jouret

2 joint publications

Matthieu Egloff

2 joint publications

Paul Kuentz

1 joint publications

Chloé Angélini