Betrand Isidor

Phenotype delineation of <i>ZNF462</i> related syndrome

Paul Kruszka, Tommy Hu, Sung‐Kook Hong et al. · American Journal of Medical Genetics Part A · 2019 · 37 citations · Full text

Distinct phenotype of PHF6 deletions in females

Nataliya Di Donato, Betrand Isidor, Serena Lopez Cazaux et al. · European Journal of Medical Genetics · 2014 · 19 citations

Genetic Disorder, Genetics, Molecular Genetics +5

The use of procalcitonin in the diagnosis of late-onset infection in neonatal intensive care unit patients

Betrand Isidor, Gaëlle Caillaux, Valérie Gilquin et al. · Scandinavian Journal of Infectious Diseases · 2007 · 17 citations

Neonatology, Diagnosis, Critical Care Medicine +17

<i>SEMA6B</i> variants cause intellectual disability and alter dendritic spine density and axon guidance

Amélie Cordovado, Martina Schaettin, Médéric Jeanne et al. · Human Molecular Genetics · 2022 · 15 citations · Full text

Axon Guidance, Neurological Disorder, Genetics +20