| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A gene homologous to plasminogen located on human chromosome 2q11–p11
|
Frank, Susan Lynn
|
|
1989
|
4 |
3 |
p. 449-451
3 p.
|
artikel
|
| 2 |
Analysis of somatic mutations at human minisatellite loci in tumors and cell lines
|
Armour, John A.L.
|
|
1989
|
4 |
3 |
p. 328-334
7 p.
|
artikel
|
| 3 |
A physical map including a new class I gene (cda12) of the human major histocompatibility complex ( A2 B13 haplotype) derived from a monosomy 6 mutant cell line
|
Ragoussis, Jiannis
|
|
1989
|
4 |
3 |
p. 301-308
8 p.
|
artikel
|
| 4 |
Assignment of the feline α-l-iduronidase gene to chromosome D4
|
Schuchman, Edward H.
|
|
1989
|
4 |
3 |
p. 442-444
3 p.
|
artikel
|
| 5 |
Assignment of the human intestinal Na+/glucose cotransporter gene (SGLT1) to the q11.2 → qter region of chromosome 22
|
Hediger, Matthias A.
|
|
1989
|
4 |
3 |
p. 297-300
4 p.
|
artikel
|
| 6 |
Characterization of a nondeleterious L1 insertion in an intron of the human factor VIII gene and further evidence of open reading frames in functional L1 elements
|
Woods-Samuels, Patricia
|
|
1989
|
4 |
3 |
p. 290-296
7 p.
|
artikel
|
| 7 |
Chromosomal localization of human genes required for G1 progression in mammalian cells
|
Greco, Angela
|
|
1989
|
4 |
3 |
p. 240-245
6 p.
|
artikel
|
| 8 |
Chromosomal localization of zinc finger protein genes in man and mouse
|
Ashworth, Alan
|
|
1989
|
4 |
3 |
p. 323-327
5 p.
|
artikel
|
| 9 |
Complete structure of the gene for human keratin 18
|
Kulesh, David A.
|
|
1989
|
4 |
3 |
p. 339-347
9 p.
|
artikel
|
| 10 |
Definition of subchromosomal intervals around the myotonic dystrophy gene region at 19q
|
Schonk, Dominique
|
|
1989
|
4 |
3 |
p. 384-396
13 p.
|
artikel
|
| 11 |
Development of multiple endocrine neoplasia type 2A does not involve substantial deletions of chromosome 10
|
Landsvater, R.M.
|
|
1989
|
4 |
3 |
p. 246-250
5 p.
|
artikel
|
| 12 |
Genomic organization of human 5 S rDNA and sequence of one tandem repeat
|
Little, Randall D.
|
|
1989
|
4 |
3 |
p. 376-383
8 p.
|
artikel
|
| 13 |
Isolation and chromosomal localization of the human En-2 gene
|
Poole, Stephen J.
|
|
1989
|
4 |
3 |
p. 225-231
7 p.
|
artikel
|
| 14 |
Isolation and field-inversion gel electrophoresis analysis of DNA markers located close to the Huntington disease gene
|
Pritchard, C.A.
|
|
1989
|
4 |
3 |
p. 408-418
11 p.
|
artikel
|
| 15 |
Isolation and restriction map of the V-J interval of the human T cell receptor γ chain locus
|
Fox, Victor L.
|
|
1989
|
4 |
3 |
p. 445-448
4 p.
|
artikel
|
| 16 |
Linkage analysis of multiple endocrine neoplasia type 1 with INT2 and other markers on chromosome 11
|
Bale, Sherri J.
|
|
1989
|
4 |
3 |
p. 320-322
3 p.
|
artikel
|
| 17 |
Localization of the gene for classic Alport syndrome
|
Flinter, Frances A.
|
|
1989
|
4 |
3 |
p. 335-338
4 p.
|
artikel
|
| 18 |
Localization of the human erbB-2 gene on normal and rearranged chromosomes 17 to bands q12–21.32
|
Popescu, Nicholas C.
|
|
1989
|
4 |
3 |
p. 362-366
5 p.
|
artikel
|
| 19 |
Mapping and characterization of an X-linked processed gene related to MYCL1
|
Morton, Cynthia C.
|
|
1989
|
4 |
3 |
p. 367-375
9 p.
|
artikel
|
| 20 |
Mapping the short arm of human chromosome 16
|
Callen, D.F.
|
|
1989
|
4 |
3 |
p. 348-354
7 p.
|
artikel
|
| 21 |
Molecular cloning and mapping of the ecotropic leukemia provirus Emv-23 provides molecular access to the albino-deletion complex in mouse chromosome 7
|
Rinchik, Eugene M.
|
|
1989
|
4 |
3 |
p. 251-258
8 p.
|
artikel
|
| 22 |
Molecular structure of the human asparagine synthetase gene
|
Zhang, Yi Ping
|
|
1989
|
4 |
3 |
p. 259-265
7 p.
|
artikel
|
| 23 |
Mutations in the catalytic domain of human coagulation factor IX: Rapid characterization by direct genomic sequencing of DNA fragments displaying an altered melting behavior
|
Attree, Oliver
|
|
1989
|
4 |
3 |
p. 266-272
7 p.
|
artikel
|
| 24 |
Neuroblastoma double minutes isolated by pulsed-field gel electrophoresis without prior strand-cleaving treatments
|
Chen, Terence L.
|
|
1989
|
4 |
3 |
p. 430-433
4 p.
|
artikel
|
| 25 |
Nucleotide sequence comparison of five human pepsinogen A (PGA) genes: Evolution of the PGA multigene family
|
Evers, M.P.J.
|
|
1989
|
4 |
3 |
p. 232-239
8 p.
|
artikel
|
| 26 |
Organization of the exons coding for pro α1(II) collagen N-propeptide confirms a distinct evolutionary history of this domain of the fibrillar collagen genes
|
Su, Ming-Wan
|
|
1989
|
4 |
3 |
p. 438-441
4 p.
|
artikel
|
| 27 |
Segregation of the Huntington disease region of human chromosome 4 in a somatic cell hybrid
|
Cox, D.R.
|
|
1989
|
4 |
3 |
p. 397-407
11 p.
|
artikel
|
| 28 |
Synteny on mouse chromosome 5 of homologs for human DNA loci linked to the Huntington disease gene
|
Cheng, Shirley V.
|
|
1989
|
4 |
3 |
p. 419-426
8 p.
|
artikel
|
| 29 |
The distribution of interspersed repetitive DNA sequences in the human genome
|
Moyzis, Robert K.
|
|
1989
|
4 |
3 |
p. 273-289
17 p.
|
artikel
|
| 30 |
The DNF15S2 locus at 3p21 is transcribed in normal lung and small cell lung cancer
|
Naylor, S.L.
|
|
1989
|
4 |
3 |
p. 355-361
7 p.
|
artikel
|
| 31 |
The gene for incontinentia pigmenti is assigned to Xq28
|
Sefiani, A.
|
|
1989
|
4 |
3 |
p. 427-429
3 p.
|
artikel
|
| 32 |
The human calbindin 27-kDa gene: Structural organization of the 5′ and 3′ regions, chromosomal assignment, and restriction fragment length polymorphism
|
Parmentier, M.
|
|
1989
|
4 |
3 |
p. 309-319
11 p.
|
artikel
|
| 33 |
Three-point linkage analysis using multiple DNA polymorphic markers in families with X-linked nephrogenic diabetes insipidus
|
Knoers, N.
|
|
1989
|
4 |
3 |
p. 434-437
4 p.
|
artikel
|
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