Results
|
|
1.
|
|
|
|
2.
|
|
|
|
3.
|
|
|
|
4.
|
|
|
|
5.
|
|
|
|
6.
|
|
|
|
7.
|
|
|
|
8.
|
|
|
|
9.
|
|
|
|
10.
|
|
|
|
11.
|
|
|
|
12.
|
|
|
|
13.
|
|
|
|
14.
|
|
|
|
15.
|
|
|
|
16.
|
|
|
|
17.
|
|
|
|
18.
|
|
|
|
19.
|
Loss of CRB2 in Müller glial cells modifies a CRB1-associated retinitis pigmentosa phenotype into a Leber congenital amaurosis phenotype. [electronic resource] by
- Quinn, Peter M
- Mulder, Aat A
- Henrique Alves, C
- Desrosiers, Mélissa
- de Vries, Sharon I
- Klooster, Jan
- Dalkara, Deniz
- Koster, Abraham J
- Jost, Carolina R
- Wijnholds, Jan
Producer: 20190614
In:
Human molecular genetics vol. 28
Availability: No items available.
|
|
|
20.
|
Oncogenomic analysis of mycosis fungoides reveals major differences with Sezary syndrome. [electronic resource] by
- van Doorn, Remco
- van Kester, Marloes S
- Dijkman, Remco
- Vermeer, Maarten H
- Mulder, Aat A
- Szuhai, Karoly
- Knijnenburg, Jeroen
- Boer, Judith M
- Willemze, Rein
- Tensen, Cornelis P
Producer: 20090206
In:
Blood vol. 113
Availability: No items available.
|