I. Garin
发表
B. Gener,
E. Anda,
R. Rodríguez-López,
2018,
BMC Medical Genetics.
C. Largo,
M. Bastepe,
E. Fernandez-Rebollo,
2010,
The Journal of clinical endocrinology and metabolism.
I. Urrutia,
L. Castaño,
R. Martínez,
2014,
Journal of pediatric endocrinology & metabolism : JPEM.
César Martín,
O. Hiort,
E. Fernandez-Rebollo,
2011,
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.
S. Elalaoui,
A. Sefiani,
G. Pérez de Nanclares,
2013,
Molecular Syndromology.
J. Clarke,
C. Kannengiesser,
A. Linglart,
2015,
The Journal of clinical endocrinology and metabolism.
E. Fernandez-Rebollo,
L. Castaño,
Guiomar Pérez de Nanclares,
2009,
European journal of endocrinology.
G. Perez de Nanclares,
I. Guerra,
M. Vicente,
2013,
The Journal of clinical endocrinology and metabolism.
E. Fernandez-Rebollo,
F. Goñi,
L. Castaño,
2010
.
B. Decallonne,
A. Martin-Trujillo,
D. Monk,
2016,
Clinical Epigenetics.
A. Barlier,
U. Aguirre,
K. Freson,
2014,
European Journal of Human Genetics.
Recessive mutations in the INS gene result in neonatal diabetes through reduced insulin biosynthesis
A. Hattersley,
S. Ellard,
L. Harries,
2010,
Proceedings of the National Academy of Sciences.
A. Linglart,
C. Silve,
C. Thomas-Teinturier,
2016,
American journal of medical genetics. Part A.
G. Perez de Nanclares,
Javier Errea-Dorronsoro,
I. Garin,
2018,
Clinical endocrinology.
A. Barlier,
O. Hiort,
K. Freson,
2016,
European journal of endocrinology.
A. Linglart,
G. Perez de Nanclares,
V. Grybek,
2016,
The Journal of clinical endocrinology and metabolism.
A. Linglart,
C. Silve,
F. Elli,
2013,
European Journal of Human Genetics.
E. Fernandez-Rebollo,
I. Rica,
L. Castaño,
2008,
Clinical endocrinology.
T. Eggermann,
D. Mackay,
K. Buiting,
2015,
Biomolecular concepts.
P. Lapunzina,
D. Monk,
F. Court,
2013,
Human mutation.
B. Gener,
G. Perez de Nanclares,
M. García-Barcina,
2013,
Orphanet Journal of Rare Diseases.
F. Martínez,
P. Lapunzina,
E. Fernandez-Rebollo,
2012,
The Journal of clinical endocrinology and metabolism.
E. Fernandez-Rebollo,
F. Goñi,
L. Castaño,
2010,
European journal of endocrinology.
A. Barlier,
U. Aguirre,
K. Freson,
2015,
European Journal of Human Genetics.
E. Fernandez-Rebollo,
L. Castaño,
R. Barrio,
2008,
Clinical endocrinology.
B. Decallonne,
A. Martin-Trujillo,
D. Monk,
2016,
Clinical Epigenetics.
E. Ars,
M. García-González,
J. Ballarín,
2018,
American journal of kidney diseases : the official journal of the National Kidney Foundation.
L. Harries,
Ó. Rubio-Cabezas,
L. Castaño,
2012,
PloS one.
Hypomethylation of the KCNQ1OT1 imprinting center of chromosome 11 associated to Sotos-like features
M. Roselló,
C. Orellana,
F. Martínez,
2012,
Journal of Human Genetics.
B. Gener,
B. Lecumberri,
I. Garin,
2014,
Journal of Pediatric Endocrinology & Metabolism (JPEM).
I. Rica,
L. Castaño,
A. Aguayo,
2010,
Journal of pediatric endocrinology & metabolism : JPEM.
S. Carrera,
E. Beristain,
A. Sancho,
2017
.
G. Perez de Nanclares,
J. Sánchez del Pozo,
I. Garin,
2017,
American journal of medical genetics. Part A.
H. Maortua,
Cristina Martínez,
S. Carrera,
2023,
Hereditary Cancer in Clinical Practice.
J. Argente,
S. Shyng,
L. Castaño,
2010,
The Journal of clinical endocrinology and metabolism.
L. Castaño,
G. Pérez de Nanclares,
R. Martínez,
2009,
Diabetic medicine : a journal of the British Diabetic Association.
A. Barlier,
O. Hiort,
K. Freson,
2016
.
M. Moreno-García,
J. S. del Pozo,
I. Garin,
2010,
American journal of medical genetics. Part A.
D. Monk,
Ana Monteagudo-Sánchez,
I. Garin,
2018,
Methods in molecular biology.
Recessive mutations in the INS gene result in neonatal diabetes through reduced insulin biosynthesis
A. Hattersley,
S. Ellard,
L. Harries,
2010,
Proceedings of the National Academy of Sciences of the United States of America.