Results
|
|
441.
|
|
|
|
442.
|
|
|
|
443.
|
|
|
|
444.
|
|
|
|
445.
|
|
|
|
446.
|
|
|
|
447.
|
|
|
|
448.
|
|
|
|
449.
|
|
|
|
450.
|
|
|
|
451.
|
ALMS1 null mutations: a common cause of Leber congenital amaurosis and early-onset severe cone-rod dystrophy. [electronic resource] by
- Xu, Y
- Guan, L
- Xiao, X
- Zhang, J
- Li, S
- Jiang, H
- Jia, X
- Yin, Y
- Guo, X
- Wang, J
- Zhang, Q
Publication details: Clinical genetics Apr 2016
In:
Clinical genetics vol. 89
Availability: No items available.
|
|
|
452.
|
|
|
|
453.
|
|
|
|
454.
|
|
|
|
455.
|
|
|
|
456.
|
A large multiexonic genomic deletion within the ALMS1 gene causes Alström syndrome in a consanguineous Pakistani family. [electronic resource] by
- Nikopoulos, K
- Butt, G U
- Farinelli, P
- Mudassar, M
- Domènech-Estévez, E
- Samara, C
- Kausar, M
- Masroor, I
- Chrast, R
- Rivolta, C
- Siddiqi, S
Publication details: Clinical genetics Apr 2016
In:
Clinical genetics vol. 89
Availability: No items available.
|
|
|
457.
|
|
|
|
458.
|
|
|
|
459.
|
|
|
|
460.
|
|