| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A genetic linkage map of five marker loci in and around the Duchenne muscular dystrophy locus
|
Chen, J.D.
|
|
1989
|
4 |
1 |
p. 105-109
5 p.
|
artikel
|
| 2 |
A genetic linkage map of the long arm of human chromosome 22
|
Rouleau, Guy A.
|
|
1989
|
4 |
1 |
p. 1-6
6 p.
|
artikel
|
| 3 |
A 1.5-Megabase restriction map surrounding MYC does not include the translocation breakpoint in familial renal cell carcinoma
|
Gemmill, Robert M.
|
|
1989
|
4 |
1 |
p. 28-35
8 p.
|
artikel
|
| 4 |
cDNA Sequence, interspecies comparison, and gene mapping analysis of argininosuccinate lyase
|
Todd, S.
|
|
1989
|
4 |
1 |
p. 53-59
7 p.
|
artikel
|
| 5 |
Chromosomal localization of the human gene for brain Ca2+ calmodulin -dependent protein kinase type IV
|
Sikela, James M.
|
|
1989
|
4 |
1 |
p. 21-27
7 p.
|
artikel
|
| 6 |
Chromosomal mapping of the mouse IL-4 and human IL-5 genes
|
Takahashi, Masazumi
|
|
1989
|
4 |
1 |
p. 47-52
6 p.
|
artikel
|
| 7 |
Confirmation of linkage of Friedreich ataxia to chromosome 9 and identification of a new closely linked marker
|
Fujita, Ricardo
|
|
1989
|
4 |
1 |
p. 110-111
2 p.
|
artikel
|
| 8 |
Frequent recombination is observed in the distal end of the long arm of chromosome 14
|
Nakamura, Yusuke
|
|
1989
|
4 |
1 |
p. 76-81
6 p.
|
artikel
|
| 9 |
Human SSAV-related endogenous retroviral element: LTR-like sequence and chromosomal localization to 18q21
|
Brack-Werner, Ruth
|
|
1989
|
4 |
1 |
p. 68-75
8 p.
|
artikel
|
| 10 |
Loss of heterozygosity at chromosomal regions 3p and 13q in non-small-cell carcinoma of the lung represents low-frequency events
|
Becker, Dorothea
|
|
1989
|
4 |
1 |
p. 97-100
4 p.
|
artikel
|
| 11 |
Mapping of four translocation breakpoints within the Duchenne muscular dystrophy gene
|
Bodrug, S.E.
|
|
1989
|
4 |
1 |
p. 101-104
4 p.
|
artikel
|
| 12 |
Mapping of the human complement factor I gene to 4q25
|
Shiang, Rita
|
|
1989
|
4 |
1 |
p. 82-86
5 p.
|
artikel
|
| 13 |
Molecular heterogeneity of steroid sulfatase deficiency: A multicenter study on 57 unrelated patients, at DNA and protein levels
|
Ballabio, A.
|
|
1989
|
4 |
1 |
p. 36-40
5 p.
|
artikel
|
| 14 |
Physical fine mapping of the choroideremia locus using Xq21 deletions associated with complex syndromes
|
Cremers, Frans P.M.
|
|
1989
|
4 |
1 |
p. 41-46
6 p.
|
artikel
|
| 15 |
The gene for catalase is assigned between the antigen loci MIC4 and MIC11
|
Couillin, Philippe
|
|
1989
|
4 |
1 |
p. 7-11
5 p.
|
artikel
|
| 16 |
The human glucocerebrosidase gene and pseudogene: Structure and evolution
|
Horowitz, Mia
|
|
1989
|
4 |
1 |
p. 87-96
10 p.
|
artikel
|
| 17 |
Twenty-eight loci form a continuous linkage map of markers for human chromosome 1
|
O'Connell, P.
|
|
1989
|
4 |
1 |
p. 12-20
9 p.
|
artikel
|
| 18 |
X-Chromosome inactivation in the Wiskott-Aldrich syndrome: A marker for detection of the carrier state and identfication of cell lineages expressing the gene defect
|
Greer, Wenda L.
|
|
1989
|
4 |
1 |
p. 60-67
8 p.
|
artikel
|
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