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 |