C. Poirsier
发表
J. Melki,
A. Toutain,
A. Verloes,
2021,
Orphanet Journal of Rare Diseases.
Y. Ville,
C. Bole-Feysot,
J. Rendu,
2020,
Clinical genetics.
Nick C Fox,
W. M. van der Flier,
A. Uitterlinden,
2022,
Genome Medicine.
S. Aubert,
B. Delemer,
S. Barraud,
2021,
Endocrine.
N. Philip,
P. Calvas,
N. Lévy,
2019,
Orphanet Journal of Rare Diseases.
A. Lèbre,
M. Doco‐Fenzy,
M. Labrousse,
2019,
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology.
J. Toutain,
C. Yardin,
F. Vialard,
2015,
European Journal of Human Genetics.
C. Garel,
A. Benachi,
N. Girard,
2023,
Prenatal diagnosis.
A. Afenjar,
A. Verloes,
C. Yardin,
2022,
American journal of medical genetics. Part A.
A. Lèbre,
O. Beaudoux,
E. Canivet,
2021,
American journal of medical genetics. Part A.
A. Toutain,
N. Philip,
P. Jouk,
2023,
BMC Health Services Research.
B. Drénou,
S. Coutant,
N. Elçioglu,
2021,
Journal of Medical Genetics.
V. Cottin,
A. Lèbre,
M. Doco‐Fenzy,
2020,
Biology.
P. Fergelot,
F. Alkuraya,
P. Bayrak-Toydemir,
2023,
Journal of Medical Genetics.
A. Afenjar,
A. Verloes,
C. Yardin,
2022,
American Journal of Medical Genetics Part A.
Nikita R. Dsouza,
Magalie S Leduc,
J. Graham,
2022,
Genome Medicine.
M. Doco‐Fenzy,
N. Bednarek,
D. Gaillard,
2014,
European journal of medical genetics.
C. Thauvin-Robinet,
A. Bertaut,
C. Cabrol,
2023,
European Journal of Medical Genetics.
Olivier Tassy,
P. Pennamen,
C. Rooryck,
2022,
American journal of medical genetics. Part A.