C. Vaché
发表
J. Millán,
H. Bolz,
M. Claustres,
2012,
Human mutation.
E. Aller,
J. Millán,
M. Claustres,
2013,
Molecular vision.
J. Millán,
M. Claustres,
S. Malcolm,
2013,
Molecular genetics & genomic medicine.
M. Koenig,
M. Claustres,
S. Malcolm,
2016,
Human mutation.
M. Koenig,
A. Roux,
C. Hamel,
2018,
Human mutation.
M. Koenig,
R. Touraine,
M. Claustres,
2017,
Scientific Reports.
M. Koenig,
Julie Bianchi,
A. Roux,
2022,
Diagnostics.
M. Claustres,
D. Bonneau,
S. Malcolm,
2014,
Human mutation.
L. Hetterschijt,
E. van Wijk,
T. Peters,
2016,
Molecular therapy. Nucleic acids.
D. Goudie,
T. Pippucci,
R. Newbury-Ecob,
2020,
Brain : a journal of neurology.
B. Gilbert-Dussardier,
M. Claustres,
D. Lacombe,
2011,
Investigative ophthalmology & visual science.
M. Claustres,
S. Malcolm,
A. Roux,
2010,
Human mutation.
M. Claustres,
A. Roux,
S. Tuffery-Giraud,
2009,
Human mutation.
C. Vaché,
E. Clottes,
Fabrice Rossignol,
2002,
Gene.
M. Claustres,
A. Roux,
A. Janecke,
2010,
Human mutation.
P. Calvas,
M. Claustres,
S. Malcolm,
2012,
Human mutation.
L. Hetterschijt,
E. van Wijk,
T. Peters,
2016
.
Julie Bianchi,
A. Roux,
C. Vaché,
2021,
European Journal of Human Genetics.
M. Koenig,
Julie Bianchi,
A. Roux,
2021,
European Journal of Human Genetics.
B. Gilbert-Dussardier,
Julie Bianchi,
M. Claustres,
2021,
International journal of molecular sciences.
B. Dastugue,
C. Vaury,
C. Vaché,
2007,
Environmental toxicology and chemistry.
B. Dastugue,
A. Meiniel,
C. Vaury,
2006,
Environmental toxicology and chemistry.
A. Roux,
C. Blanchet,
C. Vaché,
2021,
Diagnostics.
Identification and in vivo functional investigation of a HOMER2 nonstop variant causing hearing loss
M. Cossée,
A. Roux,
G. Lina-Granade,
2023,
European Journal of Human Genetics.
M. Koenig,
A. Roux,
J. Puechberty,
2020,
Frontiers in Genetics.
J. Millán,
H. Bolz,
M. Claustres,
2012,
Human mutation.