M. Lacour
发表
S. Izui,
L. Fossati,
R. Merino,
1992,
European journal of immunology.
Homozygous nonsense mutation in helix 2 of K14 causes severe recessive epidermolysis bullosa simplex
E. Lane,
J. McGrath,
R. Eady,
1998,
Human mutation.
J. Harper,
D. Atherton,
M. Lacour,
1996,
The British journal of dermatology.
M. Lacour,
2011
.
M. Lacour,
2019
.
Buschke–Ollendorff Syndrome, Marfan Syndrome, Osteogenesis Imperfecta, Anetodermas and Atrophodermas
M. Lacour,
2011
.
G. L. La Scala,
K. Posfay‐Barbe,
M. Lacour,
2015,
Pediatric dermatology.
M. Lacour,
2019
.
A. Finlay,
M. Cork,
M. Sumner,
2000,
The British journal of dermatology.
B. Lake,
M. Lacour,
1995,
British Journal of Dermatology.
R. Auckenthaler,
S. Suter,
A. Beutler,
1991,
European Journal of Pediatrics.
S. Schurmans,
S. Izui,
L. Fossati,
1990,
European journal of immunology.
M. Lacour,
C. Coultre,
1991,
Pediatric dermatology.
M. Lacour,
1996,
Dermatology.
S. Suter,
H. Vienny,
M. Lacour,
1993,
European Journal of Pediatrics.
M. Lacour,
M. Harms,
1995,
European Journal of Pediatrics.
C. Aubé,
C. Ridereau Zins,
C Aubé,
2017,
Diagnostic and interventional imaging.
J. Harper,
S. Syed,
M. Lacour,
1996,
Archives of disease in childhood.
H. Middleton-Price,
J. Harper,
M. Lacour,
1996,
Journal of medical genetics.
J. Fixsen,
F. Haddad,
J. Harper,
1999,
Journal of pediatric orthopedics.
M. Lacour,
1994,
Dermatology.
S. Meggitt,
J. Harper,
M. Lacour,
2002,
The British journal of dermatology.