A. Guerrot
发表
W. Reardon,
R. Touraine,
A. Afenjar,
2017,
Clinical genetics.
C. Verney,
P. Gressens,
S. Peineau,
2010,
Journal of Neural Transmission.
Arnold Munnich,
Patrick Nitschke,
Alice Goldenberg,
2012,
American journal of human genetics.
A. Afenjar,
T. Roscioli,
A. Verloes,
2018,
neurogenetics.
D. Campion,
O. Guillin,
V. Drouin‐Garraud,
2020,
Translational Psychiatry.
P. Gérardin,
A. Lebas,
B. Chaumette,
2018,
Clinical case reports.
E. Haan,
D. Lev,
F. Rivier,
2018,
Neurology: Genetics.
N. Brown,
B. D. de Vries,
W. Chung,
2021,
American journal of medical genetics. Part A.
M. Polak,
B. Gilbert-Dussardier,
C. Bénéteau,
2022,
EBioMedicine.
S. Julia,
R. Touraine,
A. Toutain,
2017,
American journal of medical genetics. Part C, Seminars in medical genetics.
Integrative approach to interpret DYRK1A variants, leading to a frequent neurodevelopmental disorder
R. Weksberg,
N. Drouot,
Y. Hérault,
2021,
Genetics in Medicine.
S. Marret,
S. Bekri,
L. Burglen,
2022,
Journal of clinical medicine.
A. Laquérriere,
T. Frebourg,
O. Quenez,
2016,
American journal of medical genetics. Part A.
A. Afenjar,
N. Philip,
V. Cormier-Daire,
2019,
Genetics in Medicine.
R. Pfundt,
A. Toutain,
N. Philip,
2016,
American journal of medical genetics. Part A.
A. Laquérriere,
A. Verloes,
T. Frebourg,
2016,
Prenatal diagnosis.
W. Chung,
A. Munnich,
B. Menten,
2021,
Human Genetics.
R. Pfundt,
V. Shashi,
T. Kleefstra,
2021,
American journal of medical genetics. Part A.
S. Julia,
E. Pasmant,
A. Sabbagh,
2021,
Cancers.
R. Touraine,
A. Afenjar,
A. Toutain,
2019,
Journal of Medical Genetics.
S. Marret,
A. Guerrot,
S. Rondeau,
2015,
PloS one.
S. Coutant,
F. Lecoquierre,
S. Marret,
2021,
Life.
H. Galehdari,
T. Frebourg,
R. Maroofian,
2020,
European journal of medical genetics.
Jean-François Deleuze,
Gaël Nicolas,
Anne Boland,
2019,
Clinical chemistry.
R. Touraine,
T. Frebourg,
J. Roume,
2016,
Journal of neuromuscular diseases.
R. Touraine,
J. Mandel,
J. Thevenon,
2020,
Journal of Medical Genetics.
H. Mefford,
G. Cooper,
N. Paul,
2019,
American journal of human genetics.
L. Faivre,
C. Philippe,
C. Thauvin-Robinet,
2018,
Clinical genetics.
S. Julia,
A. Afenjar,
A. Toutain,
2016,
Clinical genetics.
A. Munnich,
S. Julia,
A. Toutain,
2019,
Genetics in Medicine.
F. Lecoquierre,
M. Kilberg,
S. Bekri,
2022,
International journal of molecular sciences.
S. Marret,
A. Guerrot,
D. Pinquier,
2013,
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.
C. Bole-Feysot,
J. Steffann,
J. Pedespan,
2017,
neurogenetics.
S. Amselem,
P. Quartier,
B. Copin,
2022,
Arthritis & rheumatology.
S. Marret,
A. Guerrot,
S. Rondeau,
2012,
Acta paediatrica.
C. Rooryck,
L. Pasquier,
E. Colin,
2023,
Frontiers in Genetics.
C. Depienne,
A. Afenjar,
A. Jezela-Stanek,
2020,
Epilepsia.
N. Drouot,
A. Boland,
O. Quenez,
2023,
Human Genetics.
A. Toutain,
N. Philip,
P. Jouk,
2023,
BMC Health Services Research.
S. Marret,
J. Benoist,
S. Bekri,
2017,
International journal of molecular sciences.
Jill A. Madden,
J. Rosenfeld,
J. R. Younce,
2023,
medRxiv.
J. Thevenon,
S. Mercier,
L. Faivre,
2023,
Frontiers in Genetics.
A. Afenjar,
N. Philip,
V. Cormier-Daire,
2019,
Genetics in Medicine.
S. Moutton,
M. Rio,
Y. Lerosey,
2023,
International journal of pediatric otorhinolaryngology.
A. Boland,
T. Frebourg,
O. Quenez,
2019,
American journal of medical genetics. Part A.
S. Julia,
A. Afenjar,
A. Toutain,
2016,
Clinical genetics.
C. Depienne,
O. Guillin,
A. Afenjar,
2023,
European journal of human genetics : EJHG.
N. Brown,
B. D. de Vries,
W. Chung,
2022,
American journal of medical genetics. Part A.
A. Afenjar,
A. Bayat,
L. Pasquier,
2023,
American journal of medical genetics. Part A.