Florian Petit

Universite Lyon 1, Villeurbanne, Auvergne-Rhône-Alpes, France

Thomas Preat	grad student	2002	Universite Lyon 1
(Etude génétique de la mémoire à long terme chez Drosophila melanogaster : identification et caractérisation du gène crammer)

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Shimojima K, Narai S, Togawa M, et al. (2016) 7p22.1 microdeletions involving ACTB associated with developmental delay, short stature, and microcephaly. European Journal of Medical Genetics
Armanet N, Metay C, Brisset S, et al. (2015) Double Xp11.22 deletion including SHROOM4 and CLCN5 associated with severe psychomotor retardation and Dent disease. Molecular Cytogenetics. 8: 8
Doco-Fenzy M, Leroy C, Schneider A, et al. (2014) Early-onset obesity and paternal 2pter deletion encompassing the ACP1, TMEM18, and MYT1L genes. European Journal of Human Genetics : Ejhg. 22: 471-9
Demeer B, Andrieux J, Receveur A, et al. (2013) Duplication 16p13.3 and the CREBBP gene: confirmation of the phenotype. European Journal of Medical Genetics. 56: 26-31
Jacquemont S, Reymond A, Zufferey F, et al. (2011) Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus. Nature. 478: 97-102
Petit F, Andrieux J, Holder-Espinasse M, et al. (2011) Xq12q13.1 microduplication encompassing the EFNB1 gene in a boy with congenital diaphragmatic hernia. European Journal of Medical Genetics. 54: e525-7
Comas D, Petit F, Preat T. (2004) Drosophila long-term memory formation involves regulation of cathepsin activity. Nature. 430: 460-3