Publications by authors named "Pascale Sabeh"

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Mild phenotypes in patients with different deletions in the 3' enhancer region of SHOX.
Valancy Miranda, Pascale Sabeh, Cristian Seiltgens, Sirinart Molidperee, Chantal Janelle

Eur J Hum Genet· December 2025

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Heterozygous UBR5 variants result in a neurodevelopmental syndrome with developmental delay, autism, and intellectual disability.
Pascale Sabeh, Samantha A Dumas, Claudia Maios, Hiba Daghar, Marek Korzeniowski

Am J Hum Genet· January 2025

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Superior Performance in Prone in Infants With Congenital Heart Disease Predicts an Earlier Onset of Walking.
Lynn Dagenais, Manuela Materassi, Beatrice Desnous, Marie-Claude Vinay, Amélie Doussau, Pascale Sabeh

J Child Neurol· December 2018

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