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Andrology|February 14, 2014
A specific CBP/p300-dependent gene expression programme drives the metabolic remodelling in late stages of spermatogenesisF Boussouar, A Goudarzi, T Buchou, et al.
Prenatal Diagnosis|March 1, 2000
Successful preimplantation genetic diagnosis for sex Link Lesch--Nyhan Syndrome using specific diagnosisP F Ray, J C Harper, A Ao, et al.
Prenatal Diagnosis|February 17, 2001
First specific preimplantation genetic diagnosis for ornithine transcarbamylase deficiencyP F Ray, N Gigarel, J P Bonnefont, et al.
Thrombosis and Haemostasis|August 9, 2014
Impact of anatomical location of lower limb venous thrombus on the risk of subsequent cancerJ-P Galanaud, A C Arnoult, M-A Sevestre, et al.
Journal of Medical Genetics|September 13, 2005
Analysis of mtDNA variant segregation during early human embryonic development: a tool for successful NARP preimplantation diagnosisJ Steffann, N Frydman, N Gigarel, et al.
Human Reproduction (Oxford, England)|April 30, 2026
Single-cell proteomics reveals cytoplasmic defects in Patl2-deficient oocytes rescued by spindle transferA Cardona Barberán, E Araftpoor, A Christodoulaki, et al.
Journal of Controlled Release : Official Journal of the Controlled Release Society|December 3, 2014
Fate of inhaled monoclonal antibodies after the deposition of aerosolized particles in the respiratory systemL Guilleminault, N Azzopardi, C Arnoult, et al.
Clinical and Translational Gastroenterology|November 3, 2018
Clinical Heterogeneity of Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked Syndrome: A French Multicenter Retrospective StudyR Duclaux-Loras, F Charbit-Henrion, B Neven, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|October 14, 2017
Diagnostic yield of chromosomal microarray analysis in fetuses with isolated increased nuchal translucency: a French multicenter studyM Egloff, B Hervé, T Quibel, et al.
Clinical Genetics|October 21, 2016
Xq28 duplication including MECP2 in six unreported affected females: what can we learn for diagnosis and genetic counselling?S El Chehadeh, R Touraine, F Prieur, et al.
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