Clémence Vanlerberghe

8PUBLICATIONS
23CO-AUTHORS
Photonics, optoelectronics and optical communicationsOptical technologyGene mappingCardiology (incl. cardiovascular diseases)Adolescent health
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Publications (8)

|Aug 14, 2023
Low risk of embryonic and other cancers in PIK3CA-related overgrowth spectrum: Impact on screening recommendations.

Laurence Faivre, Jean-Charles Crépin, Manon Réda

|Feb 16, 2022
First evidence of SOX2 mutations in Peters' anomaly: Lessons from molecular screening of 95 patients.

Bertrand Chesneau, Marion Aubert-Mucca, Félix Fremont

|Jan 04, 2020
Phenotypic spectrum of TGFB3 disease-causing variants in a Dutch-French cohort and first report of a homozygous patient.

Luisa Marsili, Eline Overwater, Nadine Hanna

|Dec 16, 2018
Holt-Oram syndrome: clinical and molecular description of 78 patients with TBX5 variants.

Clémence Vanlerberghe, Anne-Sophie Jourdain, Jamal Ghoumid

|Jan 12, 2018
Genetics of patella hypoplasia/agenesis.

C Vanlerberghe, N Boutry, F Petit

|Nov 30, 2017
19p13 microduplications encompassing NFIX are responsible for intellectual disability, short stature and small head circumference.

Aurélien Trimouille, Nada Houcinat, Marie-Laure Vuillaume

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Frequent Collaborators

3 joint publications

Florence Petit

2 joint publications

Jamal Ghoumid

2 joint publications

Nicolas Chassaing

1 joint publications

Marie-Pierre Alex-Cordier