🐜
|
Mutations in the human laminin β2 (LAMB2) gene and the associated phenotypic spectrum a
38 auth.
Verena Matejas,
Bernward Hinkes,
Faisal Alkandari,
L. Al-Gazali,
E. Annexstad,
Mehmet B. Aytac,
M. Barrow,
K. Bláhová,
D. Bockenhauer,
H. Cheong,
I. Maruniak-Chudek,
P. Cochat,
J. Dötsch,
P. Gajjar,
Raoul Hennekam,
...
Françoise Janssen,
M. Kagan,
A. Kariminejad,
Markus J. Kemper,
J. Koenig,
J. Kogan,
H. Kroes,
E. Kuwertz-Bröking,
A. Lewanda,
A. Medeira,
J. Muscheites,
P. Niaudet,
M. Pierson,
A. Saggar,
L. Seaver,
M. Suri,
A. Tsygin,
E. Wühl,
A. Zurowska,
S. Uebe,
F. Hildebrandt,
C. Antignac,
M. Zenker
|
7 |
2010 |
7 🐜
|
🦁
|
[AN UNUSUAL CONGENITAL AND FAMILIAL CONGENITAL MALFORMATIVE COMBINATION INVOLVING THE EYE AND KIDNEY].
M. Pierson,
J. Cordier,
F. Hervouuet,
G. Rauber
|
6 |
1963 |
6 🦁
|
🐢
|
[CHROMOSOME ABERRATIONS].
S. Gilgenkrantz,
D. Olive,
M. Pierson
|
6 |
1963 |
6 🐢
|
🐬
|
Demonstration of two novel LAMB2 mutations in the original Pierson syndrome family reported 42 years ago
M. Zenker,
M. Pierson,
P. Jonveaux,
A. Reis
|
5 |
2005 |
5 🐬
|
🐢
|
[Nicotine poisoning in an infant].
L. Caussade,
N. Neimann,
M. Pierson
|
4 |
1954 |
4 🐢
|
🦁
|
[Klinefelter's syndrome. Trilogy of Fallot. Teratoma of the mediastinum and early puberty].
M. Pierson,
S. Gilgenkrantz,
M. Saborio,
A. Worms
|
4 |
1975 |
4 🦁
|
🐢
|
Interstitial deletion of chromosome 15: two cases
10 auth.
L. Formiga,
L. Poenaru,
F. Couronne,
E. Flori,
J. L. Eibel,
M. Deminatti,
...
J. Savary,
J. Lai,
Simone Gilgenkrantz,
M. Pierson
|
4 |
1988 |
4 🐢
|
🐬
|
Chromosome 13q+ par translocation probable d'un Y surnuméraire.
S. Gilgenkrantz,
M. Pierson,
G. Mauuary
|
4 |
1973 |
4 🐬
|