Results
|
|
21.
|
|
|
|
22.
|
|
|
|
23.
|
|
|
|
24.
|
|
|
|
25.
|
|
|
|
26.
|
|
|
|
27.
|
Characterization of FMR1 proteins isolated from different tissues. [electronic resource] by
- Verheij, C
- de Graaff, E
- Bakker, C E
- Willemsen, R
- Willems, P J
- Meijer, N
- Galjaard, H
- Reuser, A J
- Oostra, B A
- Hoogeveen, A T
Producer: 19950914
In:
Human molecular genetics vol. 4
Availability: No items available.
|
|
|
28.
|
Characterization and localization of the FMR-1 gene product associated with fragile X syndrome. [electronic resource] by
- Verheij, C
- Bakker, C E
- de Graaff, E
- Keulemans, J
- Willemsen, R
- Verkerk, A J
- Galjaard, H
- Reuser, A J
- Hoogeveen, A T
- Oostra, B A
Producer: 19930720
In:
Nature vol. 363
Availability: No items available.
|
|
|
29.
|
Characterization of FMR1 promoter elements by in vivo-footprinting analysis. [electronic resource] by
- Schwemmle, S
- de Graaff, E
- Deissler, H
- Gläser, D
- Wöhrle, D
- Kennerknecht, I
- Just, W
- Oostra, B A
- Döerfler, W
- Vogel, W
- Steinbach, P
- Dörfler, W
Producer: 19970710
In:
American journal of human genetics vol. 60
Availability: No items available.
|
|
|
30.
|
Alternative splicing in the fragile X gene FMR1. [electronic resource] by
- Verkerk, A J
- de Graaff, E
- De Boulle, K
- Eichler, E E
- Konecki, D S
- Reyniers, E
- Manca, A
- Poustka, A
- Willems, P J
- Nelson, D L
Producer: 19930702
In:
Human molecular genetics vol. 2
Availability: No items available.
|
|
|
31.
|
Alternative splicing in the fragile X gene FMR1. [electronic resource] by
- Verkerk, A J
- de Graaff, E
- De Boulle, K
- Eichler, E E
- Konecki, D S
- Reyniers, E
- Manca, A
- Poustka, A
- Willems, P J
- Nelson, D L
Producer: 19931105
In:
Human molecular genetics vol. 2
Availability: No items available.
|
|
|
32.
|
The effect of a single base pair deletion (delta T525) and a C1634T missense mutation (pro545leu) on the expression of lysosomal alpha-glucosidase in patients with glycogen storage disease type II. [electronic resource] by
- Hermans, M M
- De Graaff, E
- Kroos, M A
- Mohkamsing, S
- Eussen, B J
- Joosse, M
- Willemsen, R
- Kleijer, W J
- Oostra, B A
- Reuser, A J
Producer: 19950413
In:
Human molecular genetics vol. 3
Availability: No items available.
|
|
|
33.
|
The full mutation in the FMR-1 gene of male fragile X patients is absent in their sperm. [electronic resource] by
- Reyniers, E
- Vits, L
- De Boulle, K
- Van Roy, B
- Van Velzen, D
- de Graaff, E
- Verkerk, A J
- Jorens, H Z
- Darby, J K
- Oostra, B
Producer: 19930916
In:
Nature genetics vol. 4
Availability: No items available.
|
|
|
34.
|
A point mutation in the FMR-1 gene associated with fragile X mental retardation. [electronic resource] by
- De Boulle, K
- Verkerk, A J
- Reyniers, E
- Vits, L
- Hendrickx, J
- Van Roy, B
- Van den Bos, F
- de Graaff, E
- Oostra, B A
- Willems, P J
Producer: 19930611
In:
Nature genetics vol. 3
Availability: No items available.
|
|
|
35.
|
|
|
|
36.
|
Segregation of FRAXE in a large family: clinical, psychometric, cytogenetic, and molecular data. [electronic resource] by
- Hamel, B C
- Smits, A P
- de Graaff, E
- Smeets, D F
- Schoute, F
- Eussen, B H
- Knight, S J
- Davies, K E
- Assman-Hulsmans, C F
- Oostra, B A
Producer: 19941130
In:
American journal of human genetics vol. 55
Availability: No items available.
|
|
|
37.
|
|
|
|
38.
|
Mental status and fragile X expression in relation to FMR-1 gene mutation. [electronic resource] by
- de Vries, B B
- Wiegers, A M
- de Graaff, E
- Verkerk, A J
- Van Hemel, J O
- Halley, D J
- Fryns, J P
- Curfs, L M
- Niermeijer, M F
- Oostra, B A
Producer: 19940929
In:
European journal of human genetics : EJHG vol. 1
Availability: No items available.
|
|
|
39.
|
FBXO7 mutations cause autosomal recessive, early-onset parkinsonian-pyramidal syndrome. [electronic resource] by
- Di Fonzo, A
- Dekker, M C J
- Montagna, P
- Baruzzi, A
- Yonova, E H
- Correia Guedes, L
- Szczerbinska, A
- Zhao, T
- Dubbel-Hulsman, L O M
- Wouters, C H
- de Graaff, E
- Oyen, W J G
- Simons, E J
- Breedveld, G J
- Oostra, B A
- Horstink, M W
- Bonifati, V
Producer: 20090210
In:
Neurology vol. 72
Availability: No items available.
|
|
|
40.
|
Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17. [electronic resource] by
- Hutton, M
- Lendon, C L
- Rizzu, P
- Baker, M
- Froelich, S
- Houlden, H
- Pickering-Brown, S
- Chakraverty, S
- Isaacs, A
- Grover, A
- Hackett, J
- Adamson, J
- Lincoln, S
- Dickson, D
- Davies, P
- Petersen, R C
- Stevens, M
- de Graaff, E
- Wauters, E
- van Baren, J
- Hillebrand, M
- Joosse, M
- Kwon, J M
- Nowotny, P
- Che, L K
- Norton, J
- Morris, J C
- Reed, L A
- Trojanowski, J
- Basun, H
- Lannfelt, L
- Neystat, M
- Fahn, S
- Dark, F
- Tannenberg, T
- Dodd, P R
- Hayward, N
- Kwok, J B
- Schofield, P R
- Andreadis, A
- Snowden, J
- Craufurd, D
- Neary, D
- Owen, F
- Oostra, B A
- Hardy, J
- Goate, A
- van Swieten, J
- Mann, D
- Lynch, T
- Heutink, P
Producer: 19980701
In:
Nature vol. 393
Availability: No items available.
|