| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to pressure palsies: a SacI polymorphism in the proximal CMT1A-REP elements may lead to genetic misdiagnosis
|
Fuchs, Christina
|
|
1998
|
2 |
1 |
p. 43-46
|
artikel
|
| 2 |
Dentatorubral-pallidoluysian atrophy or Naito-Oyanagi disease
|
Kanazawa, I.
|
|
1998
|
2 |
1 |
p. 1-17
|
artikel
|
| 3 |
Fine localization of the CMT4A locus using a PAC contig and haplotype analysis
|
Ben Othmane, Kamel
|
|
1998
|
2 |
1 |
p. 18-23
|
artikel
|
| 4 |
HLA typing in the United Kingdom multiple sclerosis genome screen
|
Coraddu, Francesca
|
|
1998
|
2 |
1 |
p. 24-33
|
artikel
|
| 5 |
Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markers
|
Hentati, Afif
|
|
1998
|
2 |
1 |
p. 55-60
|
artikel
|
| 6 |
Mapping, genomic structure, and polymorphisms of the human GABABR1 receptor gene: evaluation of its involvement in idiopathic generalized epilepsy
|
Peters, Howard Christian
|
|
1998
|
2 |
1 |
p. 47-54
|
artikel
|
| 7 |
Mutations in the Caenorhabditis elegans dystrophin-like gene dys-1 lead to hyperactivity and suggest a link with cholinergic transmission
|
Bessou, Catherine
|
|
1998
|
2 |
1 |
p. 61-72
|
artikel
|
| 8 |
Refined mapping and characterization of the recessive familial amyotrophic lateral sclerosis locus (ALS2) on chromosome 2q33
|
Hosler, Betsy A.
|
|
1998
|
2 |
1 |
p. 34-42
|
artikel
|
| 9 |
The NF2 gene and merlin protein in human osteosarcomas
|
Stemmer-Rachamimov, A. O.
|
|
1998
|
2 |
1 |
p. 73-74
|
artikel
|
| 10 |
Transcript map of the chromosome 2-linked autosomal dominant spastic paraplegia (SPG4) critical region and identification of a highly informative STRP
|
Lau, En-Lieng
|
|
1998
|
2 |
1 |
p. 75-76
|
artikel
|
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