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Plos One|June 16, 2012
Genetic polymorphisms influence the ovarian response to rFSH stimulation in patients undergoing in vitro fertilization programs with ICSIRadia Boudjenah, Denise Molina-Gomes, Antoine Torre, et al.
Analytical Chemistry|August 6, 2014
DNA analysis using an integrated microchip for multiplex PCR amplification and electrophoresis for reference samplesDelphine Le Roux, Brian E Root, Carmen R Reedy, et al.
Lab on a Chip|September 25, 2014
An integrated sample-in-answer-out microfluidic chip for rapid human identification by STR analysisDelphine Le Roux, Brian E Root, Jeffrey A Hickey, et al.
Clinical Case Reports|September 6, 2021
A novel <i>COL1A1</i> variant in a family with clinical features of hypermobile Ehlers-Danlos syndrome that proved to be a <i>COL1</i>-related overlap disorderMalika Foy, Philippe De Mazancourt, Corinne Métay, et al.
The American Journal of Pathology|December 4, 2013
Polymorphisms of human placental alkaline phosphatase are associated with in vitro fertilization success and recurrent pregnancy lossMagalie Vatin, Sylvie Bouvier, Linda Bellazi, et al.
Clinical Case Reports|March 2, 2023
A severe case of <i>PLOD1</i>-related kyphoscoliotic Ehlers-Danlos syndrome associated with several arterial and venous complications: A case reportMalika Foy, Corinne Métay, Michael Frank, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 30, 2023
A focus on dominant negative variants in a series of 170 heterozygous FXI-deficient patientsPhilippe de Mazancourt, Florence Quélin, Claire Flaujac, et al.
European Journal of Haematology|February 7, 2023
Management of rare inherited bleeding disorders: Proposals of the French Reference Centre on Haemophilia and Rare Coagulation DisordersMarc Trossaert, Valerie Chamouard, Christine Biron-Andreani, et al.
Thrombosis and Haemostasis|August 11, 2025
Whole PROC Gene Sequencing to Explain Genetically Unresolved Protein C DeficienciesLaetitia Mauge, Carla Rial, Philippe De Mazancourt, et al.
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