| no |
title |
author |
magazine |
year |
volume |
issue |
page(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
|
article
|
| 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
|
article
|
| 3 |
A genetic map of DNA loci on bovine chromosome 1
|
Barendse, William
|
|
1993
|
18 |
3 |
p. 602-608
|
article
|
| 4 |
A genetic map of index DNA loci on bovine chromosome 21
|
Barendse, William
|
|
1993
|
18 |
3 |
p. 598-601
|
article
|
| 5 |
A homologue of the Drosophila Son of Sevenless gene maps to mouse chromosome 17
|
Yulug, Isik G.
|
|
1993
|
18 |
3 |
p. 733-734
|
article
|
| 6 |
An oligonucleotide probe specific to the centromeric region of human chromosome 5
|
Gregory Matera, A.
|
|
1993
|
18 |
3 |
p. 729-731
|
article
|
| 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
|
article
|
| 8 |
A somatic cell hybrid map of human chromosome 13
|
Washington, Sarah S.
|
|
1993
|
18 |
3 |
p. 486-495
|
article
|
| 9 |
Assignment of the norepinephrine transporter protein (NET1) locusto chromosome 16
|
Gelernter, Joel
|
|
1993
|
18 |
3 |
p. 690-692
|
article
|
| 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
|
article
|
| 11 |
Author index for volume 18
|
|
|
1993
|
18 |
3 |
p. 746-748
|
article
|
| 12 |
Autosomal dominant polycystic kidney disease: Localization of the second gene to chromosome 4q13–q23
|
Kimberling, William J.
|
|
1993
|
18 |
3 |
p. 467-472
|
article
|
| 13 |
Characterization of genetic defects of hemophilia a in patients of chinese origin
|
Lin, Shu-Wha
|
|
1993
|
18 |
3 |
p. 496-504
|
article
|
| 14 |
Chromosomal localization of the human vesicularamine transporter genes
|
Peter, Doris
|
|
1993
|
18 |
3 |
p. 720-723
|
article
|
| 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
|
article
|
| 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
|
article
|
| 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
|
article
|
| 18 |
Cumulative subject index volumes 15–18
|
|
|
1993
|
18 |
3 |
p. 749-793
|
article
|
| 19 |
Definition and mapping of STSs at STR and RFLP loci in Xp11-Xq22
|
Barker, David F.
|
|
1993
|
18 |
3 |
p. 712-716
|
article
|
| 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
|
article
|
| 21 |
Fibrillin genes map to regions of conserved mouse/human syntenyon mouse chromosomes 2 and 18
|
Li, Xu
|
|
1993
|
18 |
3 |
p. 667-672
|
article
|
| 22 |
Genetic linkage of mild pseudoachondroplasia (PSACH) to markersin the pericentromeric region of chromosome 19
|
Briggs, Michael D.
|
|
1993
|
18 |
3 |
p. 656-660
|
article
|
| 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
|
article
|
| 24 |
Genomic organization and localization of the gene encoding human preprogalanin
|
Evans, Helen
|
|
1993
|
18 |
3 |
p. 473-477
|
article
|
| 25 |
Genomic organization and transcriptional units at the myotonic dystrophy locus
|
Shaw, Duncan J.
|
|
1993
|
18 |
3 |
p. 673-679
|
article
|
| 26 |
Genomic structure of and a cardiac promoter for the mousecarnitine palmitoyltransferase II gene
|
Gelb, Bruce D.
|
|
1993
|
18 |
3 |
p. 651-655
|
article
|
| 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
|
article
|
| 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
|
article
|
| 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
|
article
|
| 30 |
Identification and regional localization of a human IMPdehydrogenase-like locus (IMPDHL1) at 16p13.13
|
Doggett, Norman A.
|
|
1993
|
18 |
3 |
p. 687-689
|
article
|
| 31 |
Isolation and genetic mapping of four microsatellite repeats fromchromosome 3p21 using 40 CEPH pedigrees
|
Kumar-Singh, Rajendra
|
|
1993
|
18 |
3 |
p. 717-719
|
article
|
| 32 |
Isolation of Notl Sites from Chromosome 22q11
|
Ten Hoeve, Johanna
|
|
1993
|
18 |
3 |
p. 588-597
|
article
|
| 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
|
article
|
| 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
|
article
|
| 35 |
Linkage of typical pseudoachondroplasia to chromosome 19
|
Hecht, Jacqueline T.
|
|
1993
|
18 |
3 |
p. 661-666
|
article
|
| 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
|
article
|
| 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
|
article
|
| 38 |
Primary sequence, evolution, and repetitive elements of the Gallusgallus (chicken) β-globin cluster
|
Reitman, Marc
|
|
1993
|
18 |
3 |
p. 616-626
|
article
|
| 39 |
Regional mapping of a human rodα-transducin (GNAT1) gene to chromosome 3p22
|
Ngo, Julielani T.
|
|
1993
|
18 |
3 |
p. 724-725
|
article
|
| 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
|
article
|
| 41 |
Report of the fourth international workshop on human chromosome 21
|
Delabar, Jean-Maurice
|
|
1993
|
18 |
3 |
p. 735-745
|
article
|
| 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
|
article
|
| 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
|
article
|
| 44 |
Structural organization of the human cardiac α-myosin heavy chain gene (MYH6)
|
Epp, Trevor A.
|
|
1993
|
18 |
3 |
p. 505-509
|
article
|
| 45 |
Structure and organization of the human alpha class glutathioneS-transferase genes and related pseudogenes
|
Suzuki, Takashige
|
|
1993
|
18 |
3 |
p. 680-686
|
article
|
| 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
|
article
|
| 47 |
The gene for murine CTP: Phosphocholine cytidylyltransferase (Ctpct) is located on mouse chromosome 16
|
Rutherford, Mark S.
|
|
1993
|
18 |
3 |
p. 698-701
|
article
|
| 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
|
article
|
| 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
|
article
|
Journal description