Results
|
1.
|
|
|
2.
|
|
|
3.
|
|
|
4.
|
|
|
5.
|
|
|
6.
|
|
|
7.
|
|
|
8.
|
|
|
9.
|
|
|
10.
|
|
|
11.
|
|
|
12.
|
|
|
13.
|
|
|
14.
|
|
|
15.
|
|
|
16.
|
|
|
17.
|
|
|
18.
|
Evidence for Cholinergic Dysfunction in Autosomal Dominant Kufs Disease. [electronic resource] by
- Jarrett, Pamela
- Easton, Alexander
- Rockwood, Kenneth
- Dyack, Sarah
- McCollum, Alexander
- Siu, Victoria
- Mirsattari, Seyed M
- Massot-Tarrús, Andreu
- Beis, M Jill
- D'Souza, Nolan
- Darvesh, Sultan
Producer: 20190301
In:
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques vol. 45
Availability: No items available.
|
|
19.
|
The role of Frizzled-4 mutations in familial exudative vitreoretinopathy and Coats disease. [electronic resource] by
- Robitaille, Johane M
- Zheng, Binyou
- Wallace, Karin
- Beis, M Jill
- Tatlidil, Cuneyt
- Yang, Jenny
- Sheidow, Tom G
- Siebert, Lee
- Levin, Alex V
- Lam, Wai-Ching
- Arthur, Brian W
- Lyons, Christopher J
- Jaakkola, Elisa
- Tsilou, Ekaterini
- Williams, Charles A
- Weaver, Richard Grey
- Shields, Carol L
- Guernsey, Duane L
Producer: 20110531
In:
The British journal of ophthalmology vol. 95
Availability: No items available.
|
|
20.
|
Multilocus linkage identifies two new loci for a mendelian form of stroke, cerebral cavernous malformation, at 7p15-13 and 3q25.2-27. [electronic resource] by
- Craig, H D
- Günel, M
- Cepeda, O
- Johnson, E W
- Ptacek, L
- Steinberg, G K
- Ogilvy, C S
- Berg, M J
- Crawford, S C
- Scott, R M
- Steichen-Gersdorf, E
- Sabroe, R
- Kennedy, C T
- Mettler, G
- Beis, M J
- Fryer, A
- Awad, I A
- Lifton, R P
Producer: 19981215
In:
Human molecular genetics vol. 7
Availability: No items available.
|