| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A Physical Map of the Mouseshaker-2Region Contains Many of the Genes Commonly Deleted in Smith–Magenis Syndrome (del17p11.2p11.2)
|
Probst, Frank J.
|
|
1999
|
55 |
3 |
p. 348-352
5 p.
|
artikel
|
| 2 |
Author Index for Volume 55
|
|
|
1999
|
55 |
3 |
p. 367-368
2 p.
|
artikel
|
| 3 |
Chemokine PARC Gene (SCYA18) Generated by Fusion of Two MIP-1α/LD78α-like Genes
|
Tasaki, Yoko
|
|
1999
|
55 |
3 |
p. 353-357
5 p.
|
artikel
|
| 4 |
CHST1 and CHST2 Sulfotransferases Expressed by Human Vascular Endothelial Cells: cDNA Cloning, Expression, and Chromosomal Localization
|
Li, Xuan
|
|
1999
|
55 |
3 |
p. 345-347
3 p.
|
artikel
|
| 5 |
Cloning and Characterization of Two Cytoplasmic Dynein Intermediate Chain Genes in Mouse and Human
|
Crackower, Michael A.
|
|
1999
|
55 |
3 |
p. 257-267
11 p.
|
artikel
|
| 6 |
Cloning ofAire,the Mouse Homologue of the Autoimmune Regulator (AIRE) Gene Responsible for Autoimmune Polyglandular Syndrome Type 1 (APS1)
|
Wang, Cong-Yi
|
|
1999
|
55 |
3 |
p. 322-326
5 p.
|
artikel
|
| 7 |
Cloning of the Human Homolog of Conductin (AXIN2), a Gene Mapping to Chromosome 17q23–q24
|
Mai, Ming
|
|
1999
|
55 |
3 |
p. 341-344
4 p.
|
artikel
|
| 8 |
Comparative Mapping of Mouse and Rat Chromosomes by Fluorescencein SituHybridization
|
Grützner, Frank
|
|
1999
|
55 |
3 |
p. 306-313
8 p.
|
artikel
|
| 9 |
Genomic Organization of the Human ELF3 (ESE-1/ESX) Gene, A Member of the Ets Transcription Factor Family, and Identification of a Functional Promoter
|
Oettgen, Peter
|
|
1999
|
55 |
3 |
p. 358-362
5 p.
|
artikel
|
| 10 |
GPR56, a Novel Secretin-like Human G-Protein-Coupled Receptor Gene
|
Liu, Marjorie
|
|
1999
|
55 |
3 |
p. 296-305
10 p.
|
artikel
|
| 11 |
HumancerberusRelated GeneCER1Maps to Chromosome 9
|
Lah, M.
|
|
1999
|
55 |
3 |
p. 364-366
3 p.
|
artikel
|
| 12 |
Identification and Characterization of a Highly Conserved Protein Absent in the Alport Syndrome (A), Mental Retardation (M), Midface Hypoplasia (M), and Elliptocytosis (E) Contiguous Gene Deletion Syndrome (AMME)
|
Vitelli, Francesca
|
|
1999
|
55 |
3 |
p. 335-340
6 p.
|
artikel
|
| 13 |
Identification and Characterization of the Human Homologue (RAI2) of a Mouse Retinoic Acid-Induced Gene in Xp22
|
Walpole, Susannah M.
|
|
1999
|
55 |
3 |
p. 275-283
9 p.
|
artikel
|
| 14 |
Identification of a Locus on Distal Mouse Chromosome 12 That Controls Resistance to Tumor Necrosis Factor-Induced Lethal Shock
|
Libert, Claude
|
|
1999
|
55 |
3 |
p. 284-289
6 p.
|
artikel
|
| 15 |
Ier5,a Novel Member of the Slow-Kinetics Immediate-Early Genes
|
Williams, Max
|
|
1999
|
55 |
3 |
p. 327-334
8 p.
|
artikel
|
| 16 |
Mitotic Checkpoint LocusMAD1L1Maps to Human Chromosome 7p22 and Mouse Chromosome 5
|
Jin, Dong-Yan
|
|
1999
|
55 |
3 |
p. 363-364
2 p.
|
artikel
|
| 17 |
Molecular Cloning of MouseLrp7(Lr3) cDNA and Chromosomal Mapping of Orthologous Genes in Mouse and Human
|
Chen, David
|
|
1999
|
55 |
3 |
p. 314-321
8 p.
|
artikel
|
| 18 |
Physical Mapping of the Rippling Muscle Disease Locus
|
Stephan, Dietrich A.
|
|
1999
|
55 |
3 |
p. 268-274
7 p.
|
artikel
|
| 19 |
Sequence Analysis of Exon 8 of MAO-A Gene in Alcoholics with Antisocial Personality and Normal Controls
|
Parsian, Abbas
|
|
1999
|
55 |
3 |
p. 290-295
6 p.
|
artikel
|
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