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Publications by Florence Petit
Heterozygous Loss-Of-Function Variants of MEIS2 Cause a Triad of Palatal Defects, Congenital Heart Defects, and Intellectual Disability
European Journal of Human Genetics
Genetics
Holt-Oram Syndrome: Clinical and Molecular Description of 78 Patients With TBX5 Variants
European Journal of Human Genetics
Genetics
GnRH Regulates the Expression of Its Receptor Accessory Protein SET in Pituitary Gonadotropes
PLoS ONE
Multidisciplinary
Lessons From the Analysis of TAD Boundary Deletions in Normal Population
Somatostatin Modulation of Excitatory Synaptic Transmission Between Periventricular and Arcuate Hypothalamic Nuclei in Vitro
Journal of Neurophysiology
Neuroscience
Physiology
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