Items where authors include "Isidor, B."

Article

Cetica, V. orcid.org/0000-0001-8549-4158, Pisano, T. orcid.org/0000-0001-8920-9078, Lesca, G. orcid.org/0000-0001-7691-9492 et al. (31 more authors) (2024) Clinical and molecular characterization of patients with YWHAG‐related epilepsy. Epilepsia. ISSN 0013-9580

Taylor, J., Spiller, M., Ranguin, K. et al. (9 more authors) (2022) Expanding the phenotype of HNRNPU-related neurodevelopmental disorder with emphasis on seizure phenotype and review of literature. American Journal of Medical Genetics Part A, 188 (5). pp. 1497-1514. ISSN 1552-4825

Balasubramanian, M. orcid.org/0000-0003-1488-3695, Dingemans, A.J.M., Albaba, S. et al. (36 more authors) (2021) Comprehensive study of 28 individuals with SIN3A-related disorder underscoring the associated mild cognitive and distinctive facial phenotype. European Journal of Human Genetics, 29 (4). pp. 625-636. ISSN 1018-4813

Isidor, B., Pichon, O., Redon, R. et al. (13 more authors) (2010) Mesomelia-Synostoses Syndrome Results from Deletion of SULF1 and SLCO5A1 Genes at 8q13. American Journal of Human Genetics, 87 (1). pp. 95-100. ISSN 0002-9297