Allan Bayat
8PUBLICATIONS
106CO-AUTHORS
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Publications (8)
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|Apr 02, 2024
Mono and biallelic variants in <i>HCN2</i> cause severe neurodevelopmental disorders.Clara Houdayer, A Marie Phillips, Marie Chabbert
|Sep 23, 2023
Growth charts in DYRK1A syndrome.Pierre-Louis Lanvin, Thomas Goronflot, Bertrand Isidor
|Apr 07, 2022
Novel truncating variants in FGD1 detected in two Danish families with Aarskog-Scott syndrome and myopathic features.Allan Bayat, Bjørg Krett, Morten Dunø
|Feb 11, 2022
Phenotypic spectrum of the recurrent TRPM3 p.(Val837Met) substitution in seven individuals with global developmental delay and hypotonia.Matthew A Lines, Paula Goldenberg, Ashley Wong
|Feb 01, 2021
Phenotypic expansion of the BPTF-related neurodevelopmental disorder with dysmorphic facies and distal limb anomalies.Kevin E Glinton, Anna C E Hurst, Kevin M Bowling
|Oct 12, 2020
Expanding the phenotype of Wiedemann-Steiner syndrome: Craniovertebral junction anomalies.Sara Giangiobbe, Stefano Giuseppe Caraffi, Ivan Ivanovski
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Frequent Collaborators
2 joint publications
Ivan Ivanovski
2 joint publications
Livia Garavelli
2 joint publications
Chiara Pantaleoni
1 joint publications
Marcella Zollino
1 joint publications
Francesca Romana Lepri
1 joint publications
Martin A Mensah
1 joint publications
Jean T Pantel
1 joint publications
Dione Aguilar
1 joint publications
Omri Bar
1 joint publications
Heidi B Bentzen
