| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Adult-onset glycogen storage disease type II: phenotypic and allelic heterogeneity in German patients
|
Vorgerd, M.
|
|
1998
|
1 |
3 |
p. 205-211
|
artikel
|
| 2 |
Chromosomal localization of two genes underlying late-infantile neuronal ceroid lipofuscinosis
|
Haines, J. L.
|
|
1998
|
1 |
3 |
p. 217-222
|
artikel
|
| 3 |
Clinical and molecular genetics of primary dystonias
|
Müller, U.
|
|
1998
|
1 |
3 |
p. 165-177
|
artikel
|
| 4 |
Genetic fine mapping of the Miyoshi myopathy locus and exclusion of eight candidate genes
|
Bejaoui, K.
|
|
1998
|
1 |
3 |
p. 189-196
|
artikel
|
| 5 |
Histopathology and APOE genotype of the first Alzheimer disease patient, Auguste D.
|
Graeber, M. B.
|
|
1998
|
1 |
3 |
p. 223-228
|
artikel
|
| 6 |
Identification of two mutations and a polymorphism in the chloride channel CLCN-1 in patients with Becker's generalized myotonia
|
Esteban, Jesus
|
|
1998
|
1 |
3 |
p. 185-188
|
artikel
|
| 7 |
Lack of association between apolipoprotein E genotype and sporadic amyotrophic lateral sclerosis
|
Siddique, Teepu
|
|
1998
|
1 |
3 |
p. 213-216
|
artikel
|
| 8 |
No genetic association between the LRP receptor and sporadic or late-onset familial Alzheimer disease
|
Scott, William K.
|
|
1998
|
1 |
3 |
p. 179-183
|
artikel
|
| 9 |
Novel mutations of mitochondrial complex I in pathologically proven Parkinson disease
|
Kösel, Siegfried
|
|
1998
|
1 |
3 |
p. 197-204
|
artikel
|
| 10 |
Recent progress in the genetics of human epilepsies
|
Szepetowski, Pierre
|
|
1998
|
1 |
3 |
p. 153-163
|
artikel
|
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