| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A primer-guided nucleotide incorporation assay in the genotyping of apolipoprotein E
|
Syvänen, Ann-Christine
|
|
1990
|
8 |
4 |
p. 684-692
9 p.
|
artikel
|
| 2 |
Assignment of the human casein kinase II β-subunit gene to 6p12→p21
|
Yang-Feng, Teresa L.
|
|
1990
|
8 |
4 |
p. 741-742
2 p.
|
artikel
|
| 3 |
Author index for volume 8
|
|
|
1990
|
8 |
4 |
p. 745-747
3 p.
|
artikel
|
| 4 |
Bullous pemphigoid antigen (BPAG1): cDNA cloning and mapping of the gene to the short arm of human chromosome 6
|
Sawamura, Daisuke
|
|
1990
|
8 |
4 |
p. 722-726
5 p.
|
artikel
|
| 5 |
Characterization of the 5′-flanking region of the human and rat Na,K-ATPase α3 gene
|
Pathak, Bhavani G.
|
|
1990
|
8 |
4 |
p. 641-647
7 p.
|
artikel
|
| 6 |
Chromosome-specific subsets of human alphoid DNA identified by a chromosome 2-derived clone
|
Rocchi, Mariano
|
|
1990
|
8 |
4 |
p. 705-709
5 p.
|
artikel
|
| 7 |
Cumulative subject index volumes 6–8
|
|
|
1990
|
8 |
4 |
p. 748-772
25 p.
|
artikel
|
| 8 |
Detection of point mutations associated with genetic diseases by an exon scanning technique
|
Kaufman, Daniel L.
|
|
1990
|
8 |
4 |
p. 656-663
8 p.
|
artikel
|
| 9 |
Direct haplotyping by double digestion of PCR-amplified creatine kinase (CKMM): Application to myotonic dystrophy diagnosis
|
Lavedan, C.
|
|
1990
|
8 |
4 |
p. 739-740
2 p.
|
artikel
|
| 10 |
Gene locus for X-linked CSNB
|
Pearce, W.G.
|
|
1990
|
8 |
4 |
p. 743-
1 p.
|
artikel
|
| 11 |
Isolation of the functional human excision repair gene ERCC5 by intercosmid recombination
|
Mudgett, John S.
|
|
1990
|
8 |
4 |
p. 623-633
11 p.
|
artikel
|
| 12 |
Localization of the gene for interphotoreceptor retinoid-binding protein to mouse chromosome 14 near Np-1
|
Danciger, Michael
|
|
1990
|
8 |
4 |
p. 727-731
5 p.
|
artikel
|
| 13 |
Localization of the von Hippel-Lindau disease gene to a small region of chromosome 3
|
Hosoe, Shigeto
|
|
1990
|
8 |
4 |
p. 634-640
7 p.
|
artikel
|
| 14 |
Manic depressive illness not linked to factor IX region in an independent series of pedigrees
|
Gejman, Pablo V.
|
|
1990
|
8 |
4 |
p. 648-655
8 p.
|
artikel
|
| 15 |
Molecular characterization of Beckwith-Wiedemann syndrome (BWS) patients with partial duplication of chromosome 11p excludes the gene MYOD1 from the BWS region
|
Weksberg, R.
|
|
1990
|
8 |
4 |
p. 693-698
6 p.
|
artikel
|
| 16 |
Nucleotide sequence of the Belgian G γ+( A γδβ)0-thalassemia deletion breakpoint suggests a common mechanism for a number of such recombination events
|
Fodde, Riccardo
|
|
1990
|
8 |
4 |
p. 732-735
4 p.
|
artikel
|
| 17 |
“PCR-Karyotype” of human chromosomes in somatic cell hybrids
|
Ledbetter, Susan A.
|
|
1990
|
8 |
4 |
p. 614-622
9 p.
|
artikel
|
| 18 |
Probes for CpG islands on the distal long arm of the human X chromosome are clustered in Xq24 and Xq28
|
Maestrini, Elena
|
|
1990
|
8 |
4 |
p. 664-670
7 p.
|
artikel
|
| 19 |
Recombinations between Alu repeat sequences that result in partial deletions within the C1 inhibitor gene
|
Ariga, Tadashi
|
|
1990
|
8 |
4 |
p. 607-613
7 p.
|
artikel
|
| 20 |
Regional localization of human extracellular superoxide dismutase gene to 4pter-q21
|
Hendrickson, Dan J.
|
|
1990
|
8 |
4 |
p. 736-738
3 p.
|
artikel
|
| 21 |
Response
|
Musarella, Maria A.
|
|
1990
|
8 |
4 |
p. 743-744
2 p.
|
artikel
|
| 22 |
Structure of the human methylmalonyl-CoA mutase (MUT) locus
|
Nham, Sang-Uk
|
|
1990
|
8 |
4 |
p. 710-716
7 p.
|
artikel
|
| 23 |
Telomere-related sequences at interstitial sites in the human genome
|
Wells, Richard A.
|
|
1990
|
8 |
4 |
p. 699-704
6 p.
|
artikel
|
| 24 |
The placental ribonuclease inhibitor (RNH) gene is located on chromosome subband 11p15.5
|
Weremowicz, Stanislawa
|
|
1990
|
8 |
4 |
p. 717-721
5 p.
|
artikel
|
| 25 |
Three independent insertions of retrovirus-like sequences in the haptoglobin gene cluster of primates
|
Maeda, Nobuyo
|
|
1990
|
8 |
4 |
p. 671-683
13 p.
|
artikel
|
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