L. Bartoloni
发表
C. Foresta,
A. Ferlin,
A. Tessari,
2004,
Molecular human reproduction.
C. Foresta,
A. Ferlin,
L. Bartoloni,
2004,
Molecular human reproduction.
R. Quinton,
A. Messina,
Jacques Young,
2020,
Genetics in Medicine.
A. Roverato,
C. Foresta,
A. Bettella,
2005,
European journal of endocrinology.
A. Roverato,
C. Foresta,
A. Ferlin,
2004,
Molecular human reproduction.
J. Gilbert,
M. Pericak-Vance,
J. Vance,
2000,
Human molecular genetics.
Primary ciliary dyskinesia: a consensus statement on diagnostic and treatment approaches in children
H Omran,
A Bush,
M. Strippoli,
2009,
European Respiratory Journal.
S. Antonarakis,
R. Reinhardt,
H. Omran,
2006,
American journal of respiratory and critical care medicine.
E S Lander,
J L Blouin,
R M Gardiner,
2001,
Genomics.
Shane A. McCarthy,
Richard D Emes,
Klaudia Walter,
2017,
Nature Communications.
S. Antonarakis,
K. McElreavey,
S. Nath,
2007,
American journal of human genetics.
M. Pericak-Vance,
J. Vance,
J. Stajich,
1998,
Genomics.
C. Foresta,
A. Bettella,
A. Ferlin,
2005,
The Journal of clinical endocrinology and metabolism.
R. Carrozzo,
W. Engel,
C. Angelini,
1993,
The Journal of clinical investigation.
A. Bertomoro,
L. Bartoloni,
A. Casonato,
2006,
Thrombosis and Haemostasis.
C. Castellani,
B. Assael,
A. Tamanini,
2015,
Genetics in Medicine.
E. Falconnet,
C. Rossier,
M. D. de Santi,
2009,
Journal of Medical Genetics.
S. Antonarakis,
C. Rossier,
C. Gehrig,
2000,
Cytogenetic and Genome Research.
Ross C. Anderson,
R. Quinton,
A. Messina,
2022,
Proceedings of the National Academy of Sciences of the United States of America.
Richard D Emes,
S. Antonarakis,
G. Pals,
2013,
American journal of human genetics.
Richard D Emes,
S. Antonarakis,
G. Pals,
2013,
American journal of human genetics.
B. Dallapiccola,
T. Dottorini,
C. Foresta,
2003,
The Journal of clinical endocrinology and metabolism.
C. Foresta,
E. Moro,
A. Ferlin,
2001,
American journal of medical genetics.
C. Olcese,
L. Bartoloni,
2013
.
N. Brown,
H. Peeters,
E. Eichler,
2020,
American journal of human genetics.
S. Mundlos,
S. Antonarakis,
B. Niggemann,
2008,
Human mutation.
Miguel Armengot,
S. Antonarakis,
M. Armengot,
2002,
Proceedings of the National Academy of Sciences of the United States of America.
M. B. Pereira,
A. Need,
D. Nickerson,
2022,
Genetics in medicine : official journal of the American College of Medical Genetics.
Molecular characterization of myophosphorylase deficiency in a group of patients from Northern Italy
S. Dimauro,
C. Angelini,
M. Cadaldini,
1996,
Journal of the Neurological Sciences.
E. Falconnet,
P. Lackie,
M. Cheeseman,
2012,
Human mutation.
S. Antonarakis,
M. Armengot,
C. Gehrig,
1999,
European Journal of Human Genetics.
A. Reymond,
R. Guigó,
L. Excoffier,
2009,
Human mutation.
L. Mestroni,
M. Giacca,
F. Muntoni,
1996,
Human molecular genetics.
E. Falconnet,
C. Rossier,
M. D. de Santi,
2008,
Respiration.
M. Pericak-Vance,
W. Scott,
J. Stajich,
1998,
Journal of medical genetics.
A. Reymond,
R. Guigó,
L. Excoffier,
2022
.
S. Antonarakis,
M. Linden,
S. Eliez,
2012,
Psychiatry Research.
J. Vance,
R. Ramesar,
S. Horrigan,
1999,
Genomics.
S. Antonarakis,
B. Conrad,
M. Barker,
2007,
American journal of medical genetics. Part A.
Jasjit K. Banwait,
S. Antonarakis,
S. Deutsch,
2012,
European Journal of Human Genetics.
S. Antonarakis,
R. Lyle,
S. Vishnupriya,
2011,
Investigative ophthalmology & visual science.
S. Antonarakis,
N. Shimizu,
K. Kawasaki,
2000,
Genomics.
S. Antonarakis,
L. Bartoloni,
2004,
Pflügers Archiv.
M. Pericak-Vance,
J. Vance,
J. Stajich,
1998,
Human Heredity.
P. Duminuco,
L. Persani,
M. Bonomi,
2023,
JCI insight.
E. Falconnet,
P. Lackie,
M. Cheeseman,
2012,
Human mutation.