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Annales D'Endocrinologie|May 6, 2014
Genetic of gonadal determinationYves Morel, Florence Roucher, Delphine Mallet, et al.
Plos One|January 7, 2014
Complementarity of rotating video and underwater visual census for assessing species richness, frequency and density of reef fish on coral reef slopesDelphine Mallet, Laurent Wantiez, Soazig Lemouellic, et al.
Annales D'Endocrinologie|January 24, 2015
A late 17α-hydroxylase deficiency diagnosis that leads to the discovery of a new CYP17 gene mutationAgathe Guenego, Yves Morel, Oana Ionesco, et al.
European Journal of Pediatrics|November 16, 2011
Congenital lipoid adrenal hyperplasia (a rare form of adrenal insufficiency and ambiguous genitalia) caused by a novel mutation of the steroidogenic acute regulatory protein geneOksana Lekarev, Delphine Mallet, Tony Yuen, et al.
Annales D'Endocrinologie|May 9, 2016
Evolution of steroids during pregnancy: Maternal, placental and fetal synthesisYves Morel, Florence Roucher, Ingrid Plotton, et al.
The Journal of Clinical Endocrinology and Metabolism|October 9, 2004
Gonadal dysgenesis without adrenal insufficiency in a 46, XY patient heterozygous for the nonsense C16X mutation: a case of SF1 haploinsufficiencyDelphine Mallet, Patricia Bretones, Laurence Michel-Calemard, et al.
Plos One|March 3, 2012
Remote high-definition rotating video enables fast spatial survey of marine underwater macrofauna and habitatsDominique Pelletier, Kévin Leleu, Delphine Mallet, et al.
Frontiers in Endocrinology|October 2, 2019
Reversion SAMD9 Mutations Modifying Phenotypic Expression of MIRAGE Syndrome and Allowing Inheritance in a Usually <i>de novo</i> DisorderFlorence Roucher-Boulez, Delphine Mallet, Nicolas Chatron, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 8, 2015
A splicing mutation in the DMD gene detected by next-generation sequencing and confirmed by mRNA and protein analysisFlorence Roucher Boulez, Rita Menassa, Nathalie Streichenberger, et al.
The Journal of Clinical Endocrinology and Metabolism|May 10, 2007
Heterozygous mutation of steroidogenic factor-1 in 46,XY subjects may mimic partial androgen insensitivity syndromeRégis Coutant, Delphine Mallet, Najiba Lahlou, et al.
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