L. Jonard
发表
C. Petit,
F. Denoyelle,
V. Drouin‐Garraud,
2007,
European Journal of Human Genetics.
Ruth Rimokh,
A. Morel,
M. Rostan,
2003,
Journal of Cell Science.
H. Cavé,
A. Ziegler,
N. Loundon,
2017,
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology.
D E Goldgar,
M. Papotti,
F. Canzian,
2001,
American journal of human genetics.
C. Petit,
F. Denoyelle,
V. Drouin‐Garraud,
2006,
European Journal of Human Genetics.
B. Bader-Meunier,
I. Melki,
P. Quartier,
2013,
Pediatrics.
A. Morel,
M. Rostan,
R. Rimokh,
2003,
Journal of Cell Science.
F. Denoyelle,
A. Toutain,
M. Raynaud,
2009,
Clinical Genetics.
D. Fitzpatrick,
M. Vazquez,
R. Kooy,
2007,
American journal of medical genetics. Part A.
L. Guillot,
S. Amselem,
R. Epaud,
2012,
Human molecular genetics.
A. Rötig,
I. Durand-zaleski,
C. Florentz,
2013,
Journal of Medical Genetics.
C. Petit,
D. Weil,
J. Hardelin,
2014,
PloS one.
F. Denoyelle,
S. Lyonnet,
R. Caswell,
2022,
European journal of human genetics : EJHG.
P. Reix,
L. Guillot,
R. Epaud,
2009,
Journal of Medical Genetics.
E. Génin,
F. Denoyelle,
J. Bonnefont,
2018,
Clinical genetics.
L. Guillot,
S. Amselem,
R. Epaud,
2012,
Human molecular genetics.
Albert David,
Jean Weissenbach,
José-Alain Sahel,
2011,
Orphanet journal of rare diseases.
B. Bader-Meunier,
B. Neven,
V. Couloigner,
2013
.
P. Deltenre,
F. Denoyelle,
M. Louha,
2011,
Audiology and Neurotology Extra.
C. Petit,
F. Denoyelle,
N. Loundon,
2010,
Biochemical and biophysical research communications.
C. Bodemer,
E. Sbidian,
S. Hadj-Rabia,
2013,
Acta dermato-venereologica.
F. Giuliano,
S. Rondeau,
S. Marlin,
2020,
European journal of medical genetics.
S. Abdelhak,
L. Romdhane,
H. Ouragini,
2013,
Gene.
L. Guillot,
R. Epaud,
L. Jonard,
2012,
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.
P. Nitschké,
N. Deggouj,
A. David,
2017,
Human mutation.
C. Bodemer,
F. Denoyelle,
S. Hadj-Rabia,
2008,
European journal of medical genetics.
A. Bloch-Zupan,
H. Dollfus,
N. Loundon,
2020,
Advances in experimental medicine and biology.
F. Denoyelle,
D. Lacombe,
D. Bonneau,
2008,
American journal of medical genetics. Part A.
F. Denoyelle,
V. Drouin‐Garraud,
B. Gilbert-Dussardier,
2010,
International journal of pediatric otorhinolaryngology.
M. Abid,
S. Masmoudi,
H. Ayadi,
2013,
International journal of immunogenetics.
Olivier Sterkers,
Fanny Mochel,
Patrick Nitschke,
2017,
American journal of human genetics.
Denis Pierron,
C. Rocher,
T. Letellier,
2012,
Human mutation.
C. Petit,
F. Denoyelle,
N. Loundon,
2006,
International journal of pediatric otorhinolaryngology.
Recurrent Benign Paroxysmal Positional Vertigo in DFNB16 Patients with Biallelic STRC Gene Deletions
F. Denoyelle,
N. Loundon,
S. Marlin,
2023,
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology.
M. Vidailhet,
A. Durr,
M. Polak,
2012,
Journal of Neurology, Neurosurgery & Psychiatry.
M. Al-Haggar,
Y. Wahba,
N. Salem,
2015,
Pediatric diabetes.
A. Munnich,
F. Denoyelle,
D. Lacombe,
2016,
Human mutation.
F. Denoyelle,
C. Férec,
F. Fellmann,
2009,
European journal of medical genetics.
C. Petit,
N. Michalski,
J. Hardelin,
2013,
Gene.
T. Stojkovic,
C. Rocher,
T. Letellier,
2020,
Human molecular genetics.
H. Kremer,
F. Denoyelle,
G. Girotto,
2023,
Audiology research.
F. Denoyelle,
M. Louha,
S. Chantot-Bastaraud,
2013,
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology.
F. Denoyelle,
H. Ducou le Pointe,
J. Siffroi,
2010,
American journal of medical genetics. Part A.
A. Munnich,
H. Prokisch,
N. Boddaert,
2020,
European journal of medical genetics.
S. Moutton,
M. Rio,
Y. Lerosey,
2023,
International journal of pediatric otorhinolaryngology.
L. Guillot,
R. Epaud,
L. Jonard,
2011
.
F. Denoyelle,
M. Louha,
N. Garabedian,
2011,
Clinical Biochemistry.