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Biology|May 28, 2020
Clinical Genetics of Prolidase Deficiency: An Updated ReviewMarta Spodenkiewicz, Michel Spodenkiewicz, Maureen Cleary, et al.European Journal of Medical Genetics|August 28, 2012
Bipolar affective disorder and early dementia onset in a male patient with SHANK3 deletionKsenija Vucurovic, Emilie Landais, Cécile Delahaigue, et al.Analytical Cellular Pathology : the Journal of the European Society for Analytical Cellular Pathology|May 31, 2003
Cytogenetic evolution of human ovarian cell lines associated with chemoresistance and loss of tumorigenicityStéphanie Struski, Martine Doco-Fenzy, Michael Koehler, et al.Journal of Medical Genetics|May 28, 2011
Microtriplication of 11q24.1: a highly recognisable phenotype with short stature, distinctive facial features, keratoconus, overweight, and intellectual disabilityClaire Beneteau, Emilie Landais, Martine Doco-Fenzy, et al.Cancer Genetics|July 19, 2011
Identification of a complex 17q rearrangement in a metanephric stromal tumorJérôme Toutain, Yen VuPhi, Martine Doco-Fenzy, et al.European Journal of Human Genetics : EJHG|January 17, 2008
Molecular cytogenetic characterization of terminal 14q32 deletions in two children with an abnormal phenotype and corpus callosum hypoplasiaAnouck Schneider, Brigitte Benzacken, Agnès Guichet, et al.European Journal of Medical Genetics|February 8, 2014
Report on 3 patients with 12p duplication including GRIN2BCeline Poirsier, Emilie Landais, Nathalie Bednarek, et al.American Journal of Medical Genetics. Part A|January 18, 2006
Pure direct duplication (12)(q24.1-->q24.2) in a child with Marcus Gunn phenomenon and multiple congenital anomaliesMartine Doco-Fenzy, Pierre Mauran, Jean Marie Lebrun, et al.American Journal of Medical Genetics. Part A|April 23, 2015
A pure familial 6q15q21 split duplication associated with obesity and transmitted with partial reductionEmilie Landais, Camille Leroy, Pascale Kleinfinger, et al.Clinical Genetics|December 3, 2025
The Phenotypic Spectrum of Miller Syndrome: Insight From a French CohortMarion Aubert Mucca, Perrine Brunelle, Martine Doco Fenzy, et al.Pageof 8