Digitale Bibliotheek
Sluiten Bladeren door artikelen uit een tijdschrift
     Tijdschrift beschrijving
       Alle jaargangen van het bijbehorende tijdschrift
         Alle afleveringen van het bijbehorende jaargang
                                       Alle artikelen van de bijbehorende aflevering
 
                             49 gevonden resultaten
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
                             49 gevonden resultaten
 
 Koninklijke Bibliotheek - Nationale Bibliotheek van Nederland