A. Olry
发表
Peter N. Robinson,
H. Parkinson,
S. Köhler,
2018,
European journal of medical genetics.
Peter N. Robinson,
A. Philippakis,
M. Hurles,
2017,
American journal of human genetics.
Faye L. Bowman,
M. Brudno,
T. Groza,
2017,
Advances in experimental medicine and biology.
F. Dhombres,
A. Olry,
A. Rath,
2012,
Human mutation.
F. Dhombres,
J. Charlet,
A. Olry,
2016
.
F. Dhombres,
J. Charlet,
A. Olry,
2014
.
A. Olry,
Valérie Lanneau,
C. Rodwell,
2019,
European Journal of Human Genetics.
A. Olry,
A. Rath,
C. Gonthier,
2014,
Orphanet Journal of Rare Diseases.
A. Olry,
C. Rodwell,
A. Rath,
2020,
Orphanet Journal of Rare Diseases.
Robert W. Taylor,
A. Ballabio,
E. Bertini,
2020,
Journal of inherited metabolic disease.
A. Olry,
Valérie Lanneau,
C. Rodwell,
2019,
European Journal of Human Genetics.
Tudor Groza,
Damian Smedley,
Peter N. Robinson,
2018,
Nucleic Acids Res..
Tudor Groza,
Damian Smedley,
Peter N. Robinson,
2016,
Nucleic Acids Res..
Pieter B. T. Neerincx,
Spencer J. Gibson,
Farid Yavari Dizjikan,
2021,
European Journal of Human Genetics.
Pieter B. T. Neerincx,
Spencer J. Gibson,
Farid Yavari Dizjikan,
2021,
European Journal of Human Genetics.
Jean Charlet,
Ferdinand Dhombres,
Rémy Choquet,
2011,
ICBO.
Fiona Cunningham,
Ewan Birney,
Heidi L. Rehm,
2021
.
A. Olry,
C. Rodwell,
A. Rath,
2020,
European Journal of Human Genetics.
Pieter B. T. Neerincx,
Spencer J. Gibson,
Farid Yavari Dizjikan,
2021,
European Journal of Human Genetics.
Willie H. Chang,
Alexander X. Lozano,
M. Brudno,
2020,
Genetics in Medicine.
Annie Olry,
Ana Rath,
A. Olry,
2014,
Orphanet Journal of Rare Diseases.
Carol A. Bocchini,
Marina T. DiStefano,
E. Birney,
2022,
medRxiv.
Rachel Thompson,
Peter N Robinson,
Annie Olry,
2019,
Orphanet Journal of Rare Diseases.