nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A complete YAC contig of the Prader-Willi/Angelman chromosome region (15q11–q13) and refined localization of the SNRPN gene
|
Mutirangura, Apiwat |
|
1993 |
18 |
3 |
p. 546-552 |
artikel |
2 |
A eutherian X-linked gene, PDHA1, is autosomal in marsupials:A model for the evolution of a second, testis-specific variant in eutherian mammals
|
Fitzgerald, Jamie |
|
1993 |
18 |
3 |
p. 636-642 |
artikel |
3 |
A genetic map of DNA loci on bovine chromosome 1
|
Barendse, William |
|
1993 |
18 |
3 |
p. 602-608 |
artikel |
4 |
A genetic map of index DNA loci on bovine chromosome 21
|
Barendse, William |
|
1993 |
18 |
3 |
p. 598-601 |
artikel |
5 |
A homologue of the Drosophila Son of Sevenless gene maps to mouse chromosome 17
|
Yulug, Isik G. |
|
1993 |
18 |
3 |
p. 733-734 |
artikel |
6 |
An oligonucleotide probe specific to the centromeric region of human chromosome 5
|
Gregory Matera, A. |
|
1993 |
18 |
3 |
p. 729-731 |
artikel |
7 |
A panel of deleted mouse X chromosome somatic cell hybrids derived from the embryonic stem cell line HD3 shows preferential breakage in the Hprf-DXHX254E region
|
Arnaud, D. |
|
1993 |
18 |
3 |
p. 520-526 |
artikel |
8 |
A somatic cell hybrid map of human chromosome 13
|
Washington, Sarah S. |
|
1993 |
18 |
3 |
p. 486-495 |
artikel |
9 |
Assignment of the norepinephrine transporter protein (NET1) locusto chromosome 16
|
Gelernter, Joel |
|
1993 |
18 |
3 |
p. 690-692 |
artikel |
10 |
A transducin-like gene maps to the autosomal dominant polycystic kidney disease gene region
|
Weinstat-Saslow, Debra L. |
|
1993 |
18 |
3 |
p. 709-711 |
artikel |
11 |
Author index for volume 18
|
|
|
1993 |
18 |
3 |
p. 746-748 |
artikel |
12 |
Autosomal dominant polycystic kidney disease: Localization of the second gene to chromosome 4q13–q23
|
Kimberling, William J. |
|
1993 |
18 |
3 |
p. 467-472 |
artikel |
13 |
Characterization of genetic defects of hemophilia a in patients of chinese origin
|
Lin, Shu-Wha |
|
1993 |
18 |
3 |
p. 496-504 |
artikel |
14 |
Chromosomal localization of the human vesicularamine transporter genes
|
Peter, Doris |
|
1993 |
18 |
3 |
p. 720-723 |
artikel |
15 |
Chromosomal localization of the mouse titin gene and its relationto “muscular dystrophy with myositis” and nebulin genes on chromosome 2
|
Müller-Seitz, M. |
|
1993 |
18 |
3 |
p. 559-561 |
artikel |
16 |
Chromosomal mapping in the mouse of eight K+-channel-genes representing the four Shaker-like subfamilies Shaker, Shab, Shaw, and Shal
|
Klocke, Rainer |
|
1993 |
18 |
3 |
p. 568-574 |
artikel |
17 |
Construction and characterization of a YAC library with a lowfrequency of chimeric clones from flow-sorted human chromosome 9
|
McCormick, M.K. |
|
1993 |
18 |
3 |
p. 553-558 |
artikel |
18 |
Cumulative subject index volumes 15–18
|
|
|
1993 |
18 |
3 |
p. 749-793 |
artikel |
19 |
Definition and mapping of STSs at STR and RFLP loci in Xp11-Xq22
|
Barker, David F. |
|
1993 |
18 |
3 |
p. 712-716 |
artikel |
20 |
Detection of 98.5% of the mutations in 200 Belgian cystic fibrosis alleles by reverse dot-blot and sequencing of the complete coding region and exon/intron junctions of the CFTR gene
|
Cuppens, Harry |
|
1993 |
18 |
3 |
p. 693-697 |
artikel |
21 |
Fibrillin genes map to regions of conserved mouse/human syntenyon mouse chromosomes 2 and 18
|
Li, Xu |
|
1993 |
18 |
3 |
p. 667-672 |
artikel |
22 |
Genetic linkage of mild pseudoachondroplasia (PSACH) to markersin the pericentromeric region of chromosome 19
|
Briggs, Michael D. |
|
1993 |
18 |
3 |
p. 656-660 |
artikel |
23 |
Genetic map of the human pseudoautosomal region reveals a high rate of recombination in female meiosis at the Xp telomere
|
Henke, Anja |
|
1993 |
18 |
3 |
p. 478-485 |
artikel |
24 |
Genomic organization and localization of the gene encoding human preprogalanin
|
Evans, Helen |
|
1993 |
18 |
3 |
p. 473-477 |
artikel |
25 |
Genomic organization and transcriptional units at the myotonic dystrophy locus
|
Shaw, Duncan J. |
|
1993 |
18 |
3 |
p. 673-679 |
artikel |
26 |
Genomic structure of and a cardiac promoter for the mousecarnitine palmitoyltransferase II gene
|
Gelb, Bruce D. |
|
1993 |
18 |
3 |
p. 651-655 |
artikel |
27 |
Genomic structure of the EWS gene and its relationship to EWSR1, a site of tumor-associated chromosome translocation
|
Plougastel, Béatrice |
|
1993 |
18 |
3 |
p. 609-615 |
artikel |
28 |
Human Zn-α 2-glycoprotein: Complete genomic sequence, identification of a related pseudogene and relationship to class I major histocompatibility complex genes
|
Freije, José P. |
|
1993 |
18 |
3 |
p. 575-587 |
artikel |
29 |
Identification and analysis of the chicken c-mil promoter: Possible involvement of Sp1- and Ets-related proteins
|
Ansieau, Stéphane |
|
1993 |
18 |
3 |
p. 537-545 |
artikel |
30 |
Identification and regional localization of a human IMPdehydrogenase-like locus (IMPDHL1) at 16p13.13
|
Doggett, Norman A. |
|
1993 |
18 |
3 |
p. 687-689 |
artikel |
31 |
Isolation and genetic mapping of four microsatellite repeats fromchromosome 3p21 using 40 CEPH pedigrees
|
Kumar-Singh, Rajendra |
|
1993 |
18 |
3 |
p. 717-719 |
artikel |
32 |
Isolation of Notl Sites from Chromosome 22q11
|
Ten Hoeve, Johanna |
|
1993 |
18 |
3 |
p. 588-597 |
artikel |
33 |
Isolation of the cDNA and Chromosomal Localization of the Gene (TAX1) Encoding the Human Axonal Glycoprotein TAG-1
|
Tsiotra, Panayoula C. |
|
1993 |
18 |
3 |
p. 562-567 |
artikel |
34 |
Linkage mapping of the Aldo-2, Pax-5, Ambp, and D4H9S3Eloci on mouse chromosome 4 in the region of homology with human chromosome 9
|
Pilz, Alison |
|
1993 |
18 |
3 |
p. 705-708 |
artikel |
35 |
Linkage of typical pseudoachondroplasia to chromosome 19
|
Hecht, Jacqueline T. |
|
1993 |
18 |
3 |
p. 661-666 |
artikel |
36 |
Localization of the human growth arrest-specific gene (GAS1) to chromosome bands 9q21.3-q22, a region frequently deleted in myeloid malignancies
|
Evdokiou, Andreas |
|
1993 |
18 |
3 |
p. 731-733 |
artikel |
37 |
Mapping and cloning of the critical region for the spinocerebellar ataxia type 1 gene (SCA1) in a yeast artificial chromosome contig spanning 1.2 Mb
|
Banfi, S. |
|
1993 |
18 |
3 |
p. 627-635 |
artikel |
38 |
Primary sequence, evolution, and repetitive elements of the Gallusgallus (chicken) β-globin cluster
|
Reitman, Marc |
|
1993 |
18 |
3 |
p. 616-626 |
artikel |
39 |
Regional mapping of a human rodα-transducin (GNAT1) gene to chromosome 3p22
|
Ngo, Julielani T. |
|
1993 |
18 |
3 |
p. 724-725 |
artikel |
40 |
Regional mapping of short tandem repeats on humanchromosome 10: Cytochrome P450 gene CYP2E, D10S196, D10S220, and D10S225
|
Köble, Konrad |
|
1993 |
18 |
3 |
p. 702-704 |
artikel |
41 |
Report of the fourth international workshop on human chromosome 21
|
Delabar, Jean-Maurice |
|
1993 |
18 |
3 |
p. 735-745 |
artikel |
42 |
Single-strand conformational polymorphism (SSCP) mapping of the mouse genome: Integration of the SSCP, microsatellite, and gene maps of mouse chromosome 1
|
Hunter, Kent W. |
|
1993 |
18 |
3 |
p. 510-519 |
artikel |
43 |
Structural organization and evolution of the liver isoform gene for bovine cytochrome c oxidase subunit VIIa
|
Sathiagana Seelan, R. |
|
1993 |
18 |
3 |
p. 527-536 |
artikel |
44 |
Structural organization of the human cardiac α-myosin heavy chain gene (MYH6)
|
Epp, Trevor A. |
|
1993 |
18 |
3 |
p. 505-509 |
artikel |
45 |
Structure and organization of the human alpha class glutathioneS-transferase genes and related pseudogenes
|
Suzuki, Takashige |
|
1993 |
18 |
3 |
p. 680-686 |
artikel |
46 |
The CA repeat marker D17S791 islocated within 40 kb of the WNT3 gene on chromosome 17q
|
Chandrasekharappa, Settara C. |
|
1993 |
18 |
3 |
p. 728-729 |
artikel |
47 |
The gene for murine CTP: Phosphocholine cytidylyltransferase (Ctpct) is located on mouse chromosome 16
|
Rutherford, Mark S. |
|
1993 |
18 |
3 |
p. 698-701 |
artikel |
48 |
The human CD53 gene, coding for a four transmembrane domain protein, maps to chromosomal region 1p13
|
Eugenia Gonzalez, M. |
|
1993 |
18 |
3 |
p. 725-728 |
artikel |
49 |
The human peripheral renzodiazepine receptor gene: Cloning and characterization of alternative splicing in normal tissues and in a patient with congenital lipoid adrenal hyperplasia
|
Lin, Dong |
|
1993 |
18 |
3 |
p. 643-650 |
artikel |