Albin Blanc

2PUBLICATIONS
3CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Developmental genetics (incl. sex determination)
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Journal

Publications (2)

|May 25, 2026
Distinct Neuropsychiatric Profiles Associated With 17p11.2 Deletions and RAI1 Variants in Smith-Magenis Syndrome.

|May 07, 2024
Patient with a heterozygous pathogenic variant in CSNK2A1 gene: A new case to update the Okur-Chung neurodevelopmental syndrome.

Albin Blanc, Céline Bonnet, Marion Wandzel

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Frequent Collaborators

2 joint publications

Céline Bonnet

1 joint publications

Christophe Nemos

1 joint publications

Marie-Noëlle Babinet