| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A cosmid clone map derived from a small region of human chromosome 11
|
Harrison-Lavoie, K.J.
|
|
1989
|
5 |
3 |
p. 501-509
9 p.
|
artikel
|
| 2 |
A family of type I keratin genes and the homeobox-2 gene complex are closely linked to the rex locus on mouse chromosome 11
|
Nadeau, J.H.
|
|
1989
|
5 |
3 |
p. 454-462
9 p.
|
artikel
|
| 3 |
A multigene deletion in the human IGH constant region locus involves highly homologous hot spots of recombination
|
Keyeux, Genoveva
|
|
1989
|
5 |
3 |
p. 431-441
11 p.
|
artikel
|
| 4 |
A multipoint linkage map around the locus for myotonic dystrophy on chromosome 19
|
Brunner, H.G.
|
|
1989
|
5 |
3 |
p. 589-595
7 p.
|
artikel
|
| 5 |
Analysis of molecular deletions with cDNA probes in patients with Duchenne and Becker muscular dystrophies
|
Gilgenkrantz, H.
|
|
1989
|
5 |
3 |
p. 574-580
7 p.
|
artikel
|
| 6 |
A PstI polymorphism for the human erythrocyte surface protein band 3 (EPB3) demonstrates close linkage of EPB3 to the nerve growth factor receptor
|
Stewart, E.A.
|
|
1989
|
5 |
3 |
p. 633-635
3 p.
|
artikel
|
| 7 |
A reordering of human chromosome 19 long-arm DNA markers and identification of markers flanking the myotonic dystrophy locus
|
Korneluk, R.G.
|
|
1989
|
5 |
3 |
p. 596-604
9 p.
|
artikel
|
| 8 |
Assignment of the interleukin-2 locus to mouse chromosome 3
|
Fiorentino, Lynn
|
|
1989
|
5 |
3 |
p. 651-653
3 p.
|
artikel
|
| 9 |
At least four different chromosomal regions are involved in loss of heterozygosity in human breast carcinoma
|
Devilee, Peter
|
|
1989
|
5 |
3 |
p. 554-560
7 p.
|
artikel
|
| 10 |
Autosomal dominant retinitis pigmentosa (ADRP): Localization of an ADRP gene to the long arm of chromosome 3
|
McWilliam, Peter
|
|
1989
|
5 |
3 |
p. 619-622
4 p.
|
artikel
|
| 11 |
Autosomal dominant retinitis pigmentosa: Exclusion of a gene from extensive regions of chromosomes 6, 13, 20, and 21
|
Farrar, G.Jane
|
|
1989
|
5 |
3 |
p. 612-618
7 p.
|
artikel
|
| 12 |
Characterization of two genes for the human Na,K-ATPase β subunit
|
Lane, Lois K.
|
|
1989
|
5 |
3 |
p. 445-453
9 p.
|
artikel
|
| 13 |
Chromosomal assignment of genes encoding the α, β, and γ subunits of human complement protein C8: Identification of a close physical linkage between the α and the β loci
|
Kaufman, Kenneth M.
|
|
1989
|
5 |
3 |
p. 475-480
6 p.
|
artikel
|
| 14 |
Chromosomal localization and structure of the human P1 protamine gene
|
Krawetz, Stephen A.
|
|
1989
|
5 |
3 |
p. 639-645
7 p.
|
artikel
|
| 15 |
Chromosomal localization of DBL oncogene sequences
|
Tronick, Steven R.
|
|
1989
|
5 |
3 |
p. 546-553
8 p.
|
artikel
|
| 16 |
Chromosomal localization of murine interleukin-1 α and β genes
|
Boultwood, Jacqueline
|
|
1989
|
5 |
3 |
p. 481-485
5 p.
|
artikel
|
| 17 |
Chromosomal mapping and nucleotide sequence of a human DNA autonomously replicating sequence
|
del Pilar Aguinaga, Maria
|
|
1989
|
5 |
3 |
p. 605-611
7 p.
|
artikel
|
| 18 |
Chromosome assignment of the murine Hox-4.1 gene
|
Pravtcheva, Dimitrina
|
|
1989
|
5 |
3 |
p. 541-545
5 p.
|
artikel
|
| 19 |
Cloning and mapping of a testis-specific gene with sequence similarity to a sperm-coating glycoprotein gene
|
Kasahara, Masanori
|
|
1989
|
5 |
3 |
p. 527-534
8 p.
|
artikel
|
| 20 |
Direct sequencing of the gene for Maryland/German familial amyloidotic polyneuropathy type II and genotyping by allele-specific enzymatic amplification
|
Nichols, William C.
|
|
1989
|
5 |
3 |
p. 535-540
6 p.
|
artikel
|
| 21 |
Dispersed family of human genes with sequence similarity to farnesyl pyrophosphate synthetase
|
Heinzmann, C.
|
|
1989
|
5 |
3 |
p. 493-500
8 p.
|
artikel
|
| 22 |
Gene mapping by enzymatic amplification from flow-sorted chromosomes
|
Cotter, Finbarr
|
|
1989
|
5 |
3 |
p. 470-474
5 p.
|
artikel
|
| 23 |
Isolation of a novel mildly repetitive DNA sequence that is predominantly located at the terminus of the short arm of chromosome 4 near the Huntington disease gene
|
Altherr, Michael R.
|
|
1989
|
5 |
3 |
p. 581-588
8 p.
|
artikel
|
| 24 |
Level of expression and chromosome mapping of the mouse cholecystokinin gene: Implications for murine models of genetic obesity
|
Friedman, J.M.
|
|
1989
|
5 |
3 |
p. 463-469
7 p.
|
artikel
|
| 25 |
Linkage genetics of mouse ornithine decarboxylase (Odc)
|
Villani, Vincent
|
|
1989
|
5 |
3 |
p. 636-638
3 p.
|
artikel
|
| 26 |
Linkage of the mouse LDL receptor gene on chromosome 9
|
Frank, Susan Lynn
|
|
1989
|
5 |
3 |
p. 646-648
3 p.
|
artikel
|
| 27 |
Localization of the muscle, liver, and brain glycogen phosphorylase genes on linkage maps of mouse chromosomes 19, 12, and 2, respectively
|
Glaser, Tom
|
|
1989
|
5 |
3 |
p. 510-521
12 p.
|
artikel
|
| 28 |
Localization of three DNA segments encompassing tRNA genes to human chromosomes 1, 5, and 16: Proposed mechanism and significance of tRNA gene dispersion
|
McBride, O.Wesley
|
|
1989
|
5 |
3 |
p. 561-573
13 p.
|
artikel
|
| 29 |
Molecular cloning of a human co-β-glucosidase cDNA: Evidence that four sphingolipid hydrolase activator proteins are encoded by single genes in humans and rats
|
Rorman, Efrat Gavrieli
|
|
1989
|
5 |
3 |
p. 486-492
7 p.
|
artikel
|
| 30 |
Mouse major (γ) satellite DNA is highly conserved and organized into extremely long tandem arrays: Implications for recombination between nonhomologous chromosomes
|
Vissel, Bryce
|
|
1989
|
5 |
3 |
p. 407-414
8 p.
|
artikel
|
| 31 |
Mouse melanoma growth stimulatory activity gene (Mgsa) is polymorphic and syntenic with the W, patch, Rumpwhite, and recessive spotting loci on chromosome 5
|
Sakaguchi, Alan Y.
|
|
1989
|
5 |
3 |
p. 629-632
4 p.
|
artikel
|
| 32 |
Multilocus linkage analysis with the human argininosuccinate synthetase gene
|
Northrup, Hope
|
|
1989
|
5 |
3 |
p. 442-444
3 p.
|
artikel
|
| 33 |
Owl monkey gene map: Evidence for a homologous human chromosome 7q region near the cystic fibrosis locus
|
Ma, Nancy Shui-Fong
|
|
1989
|
5 |
3 |
p. 389-396
8 p.
|
artikel
|
| 34 |
Preferential amplification and molecular characterization of junction sequences of a pathogenetic deletion in human mitochondrial DNA
|
Johns, Donald R.
|
|
1989
|
5 |
3 |
p. 623-628
6 p.
|
artikel
|
| 35 |
Prp (proline-rich protein) genes linked to markers Es-12 (esterase-12), Ea-10 (erythrocyte alloantigen), and loci on distal mouse chromosome 6
|
Azen, Edwin A.
|
|
1989
|
5 |
3 |
p. 415-422
8 p.
|
artikel
|
| 36 |
Regional localization of the human thrombomodulin gene to 20p12-cen
|
Espinosa III, Rafael
|
|
1989
|
5 |
3 |
p. 649-650
2 p.
|
artikel
|
| 37 |
The alta summit, December 1984
|
Cook-Deegan, Robert Mullan
|
|
1989
|
5 |
3 |
p. 661-663
3 p.
|
artikel
|
| 38 |
The department of energy (DOE) human genome initiative
|
Barnhart, Benjamin J.
|
|
1989
|
5 |
3 |
p. 657-660
4 p.
|
artikel
|
| 39 |
The human genome program at the National Institutes of Health
|
Watson, James D.
|
|
1989
|
5 |
3 |
p. 654-656
3 p.
|
artikel
|
| 40 |
The mouse neurological mutant weaver maps within the region of chromosome 16 that is homologous to human chromosome 21
|
Reeves, Roger H.
|
|
1989
|
5 |
3 |
p. 522-526
5 p.
|
artikel
|
| 41 |
Transposition, amplification, and divergence in the origin of the DNF15 loci, a polymorphic repetitive sequence family on chromosomes 1 and 3
|
Welch, H.M.
|
|
1989
|
5 |
3 |
p. 423-430
8 p.
|
artikel
|
| 42 |
Two distinct areas of unequal crossingover within the steroid 21-hydroxylase genes produce absence of CYP21B
|
Donohoue, Patricia A.
|
|
1989
|
5 |
3 |
p. 397-406
10 p.
|
artikel
|
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