F. Petit

发表

F. Petit, C. Serres, J. Auer, 2014, Biochemical Society transactions.

C. Pineau, F. Petit, C. Serres, 2013, Human reproduction.

R. Carlier, P. Carlier, P. Laforêt, 2021, Neuromuscular Disorders.

J. Hogrel, P. Laforêt, J. Vissing, 2013, Molecular genetics and metabolism.

I. Nelson, E. Malfatti, N. Romero, 2017, Neurology: Genetics.

R. Carlier, P. Carlier, P. Laforêt, 2019, Muscle & nerve.

P. Laforêt, K. Wahbi, G. Ronzitti, 2020, Journal of inherited metabolic disease.

K. Clément, G. Bassez, R. Carlier, 2013, Molecular genetics and metabolism.

F. Petit, V. Gajdos, P. Labrune, 2012 .

G. Tachdjian, F. Petit, A. Aboura, 2005, European Journal of Human Genetics.

S. Bézieau, F. Petit, F. Parisot, 2008, European Journal of Human Genetics.

P. Marcorelles, F. Petit, J. Noury, 2020, Scientific Reports.

A. Benachi, A. Briand-Suleau, L. Tosca, 2015, European journal of medical genetics.

Y. Wada, J. Veltman, C. Stanley, 2014, The New England journal of medicine.

P. Laforêt, Irene J. Hoogeveen, U. Steuerwald, 2016, Journal of Inherited Metabolic Disease.

K. Claeys, J. Hogrel, P. Laforêt, 2009, The New England journal of medicine.

P. Laforêt, L. Féasson, A. Furby, 2013, Neuromuscular Disorders.

D. Rabier, P. Kamoun, J. Saudubray, 1989, Clinica chimica acta; international journal of clinical chemistry.

L. Tosca, G. Tachdjian, M. Goossens, 2010, European Journal of Human Genetics.

F. Petit, J. Brouet, S. Alain, 2004, Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology.

A. Hubert-Buron, R. Froissart, F. Petit, 2011, Orphanet journal of rare diseases.

G. Tachdjian, J. Martinovic, F. Petit, 2021, American journal of medical genetics. Part A.

F. Petit, C. Poüs, F. Parisot, 2004, Clinical genetics.

A. Benachi, L. Tosca, G. Tachdjian, 2016, Birth defects research. Part A, Clinical and molecular teratology.

F. Petit, V. Gajdos, A. Isapof, 2010, Journal of Inherited Metabolic Disease.

L. Tosca, G. Tachdjian, M. Tardieu, 2011, European journal of medical genetics.

V. Hahn-Barma, P. Laforêt, B. Eymard, 2015, Journal of Inherited Metabolic Disease.

J. Hogrel, P. Laforêt, B. Eymard, 2017, Molecular genetics and metabolism.

L. Tosca, G. Tachdjian, J. Amiel, 2018, European journal of medical genetics.

A. Echaniz-Laguna, P. Laforêt, T. Stojkovic, 2013, The Journal of clinical endocrinology and metabolism.

P. Marcorelles, F. Petit, J. Noury, 2018, Acta neurologica Scandinavica.

S. Oveisgharan, M. Mahmoudi, F. Petit, 2018, Journal of clinical neuromuscular disease.

J. Hogrel, P. Laforêt, B. Eymard, 2015, European journal of neurology.

P. Marcorelles, F. Petit, J. Noury, 2020, Scientific Reports.

E. Malfatti, N. Romero, J. Hogrel, 2012, Journal of the Neurological Sciences.

J. Hogrel, P. Laforêt, B. Eymard, 2018, Muscle & nerve.

J. Melki, M. Cossée, J. Pouget, 2018, European Journal of Human Genetics.

P. Laforêt, R. Froissart, V. Decostre, 2023, European Journal of Medical Research.

J. Bouyer, F. Petit, V. Gajdos, 2014, Clinical laboratory.

Y. Wada, J. Veltman, C. Stanley, 2014, The New England journal of medicine.