| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A YAC-Based Transcript Map of Human Chromosome 9q22.1–q22.3 Encompassing the Loci for Hereditary Sensory Neuropathy Type I and Multiple Self-Healing Squamous Epithelioma
|
Blair, Ian P.
|
|
1998
|
51 |
2 |
p. 277-281
5 p.
|
artikel
|
| 2 |
Bisulfite Sequencing in Preimplantation Embryos: DNA Methylation Profile of the Upstream Region of the Mouse ImprintedH19Gene
|
Warnecke, Peter M.
|
|
1998
|
51 |
2 |
p. 182-190
9 p.
|
artikel
|
| 3 |
cDNA Sequencing and Analysis of POV1 (PB39): A Novel Gene Up-regulated in Prostate Cancer
|
Cole, Kristina A.
|
|
1998
|
51 |
2 |
p. 282-287
6 p.
|
artikel
|
| 4 |
Characterization and Physical Mapping in Human and Mouse of a Novel RING Finger Gene in Xp22
|
Van den Veyver, Ignatia B.
|
|
1998
|
51 |
2 |
p. 251-261
11 p.
|
artikel
|
| 5 |
Characterization ofCxorf5(71-7A), a Novel Human cDNA Mapping to Xp22 and Encoding a Protein Containing Coiled-Coil α-Helical Domains
|
de Conciliis, Lisa
|
|
1998
|
51 |
2 |
p. 243-250
8 p.
|
artikel
|
| 6 |
Cloning of the Human Interferon-Related Developmental Regulator (IFRD1) Gene Coding for the PC4 Protein, a Member of a Novel Family of Developmentally Regulated Genes
|
Buanne, Pasquale
|
|
1998
|
51 |
2 |
p. 233-242
10 p.
|
artikel
|
| 7 |
CpG Islands and Double-Minute Chromosomes
|
Rizwana, Rabia
|
|
1998
|
51 |
2 |
p. 207-215
9 p.
|
artikel
|
| 8 |
Cytogenetical Assignment and Physical Mapping of the Human R-PTP-κ Gene (PTPRK) to the Putative Tumor Suppressor Gene Region 6q22.2–q22.3
|
Zhang, Yanming
|
|
1998
|
51 |
2 |
p. 309-311
3 p.
|
artikel
|
| 9 |
Differential Expansion of the N-Formylpeptide Receptor Gene Cluster in Human and Mouse
|
Gao, Ji-Liang
|
|
1998
|
51 |
2 |
p. 270-276
7 p.
|
artikel
|
| 10 |
Gene Mapping in Zebrafish Using Single-Strand Conformation Polymorphism Analysis
|
Förnzler, Dorothee
|
|
1998
|
51 |
2 |
p. 216-222
7 p.
|
artikel
|
| 11 |
Genetic Mapping of Mouse Transient Receptor Potential (Trrp) Genes Responsible for Capacitative Calcium Entry Channels to Chromosomes 3, 7, 9, and X
|
Yamazaki, Kazuto
|
|
1998
|
51 |
2 |
p. 303-305
3 p.
|
artikel
|
| 12 |
Genomic Organization and Chromosomal Localization of the HumanSGKProtein Kinase Gene
|
Waldegger, Siegfried
|
|
1998
|
51 |
2 |
p. 299-302
4 p.
|
artikel
|
| 13 |
Human Retina-Specific Amine Oxidase: Genomic Structure of the Gene (AOC2), Alternatively Spliced Variant, and mRNA Expression in Retina
|
Imamura, Yutaka
|
|
1998
|
51 |
2 |
p. 293-298
6 p.
|
artikel
|
| 14 |
Identification and Mapping of Human Histone Acetylation Modifier Gene Homologues
|
Randhawa, Gurvaneet S.
|
|
1998
|
51 |
2 |
p. 262-269
8 p.
|
artikel
|
| 15 |
Linkage Analysis and Construction of a Congenic Strain for a Blood Pressure QTL on Rat Chromosome 9
|
Rapp, John P.
|
|
1998
|
51 |
2 |
p. 191-196
6 p.
|
artikel
|
| 16 |
Physical Localization of the Mousearyl hydrocarbon receptor nuclear translocator-2(Arnt2) Gene within thec112K Deletion
|
Wines, Mary E.
|
|
1998
|
51 |
2 |
p. 223-232
10 p.
|
artikel
|
| 17 |
Recent Human-Specific Spreading of a Subtelomeric Domain
|
Monfouilloux, Sylvaine
|
|
1998
|
51 |
2 |
p. 165-176
12 p.
|
artikel
|
| 18 |
SOLH, a Human Homologue of theDrosophila melanogaster small optic lobesGene Is a Member of the Calpain and Zinc-Finger Gene Families and Maps to Human Chromosome 16p13.3 nearCATM(Cataract with Microphthalmia)
|
Kamei, Makoto
|
|
1998
|
51 |
2 |
p. 197-206
10 p.
|
artikel
|
| 19 |
Suggestive Linkage between Markers on Chromosome 19q13.2 and Nonsyndromic Orofacial Cleft Malformation
|
Martinelli, Marcella
|
|
1998
|
51 |
2 |
p. 177-181
5 p.
|
artikel
|
| 20 |
The Human CC Chemokine TECK (SCYA25) Maps to Chromosome 19p13.2
|
Nomiyama, H.
|
|
1998
|
51 |
2 |
p. 311-312
2 p.
|
artikel
|
| 21 |
The Humandead ringer/brightHomolog,DRIL1:cDNA Cloning, Gene Structure, and Mapping to D19S886, a Marker on 19p13.3 That Is Strictly Linked to the Peutz–Jeghers Syndrome
|
Kortschak, R.Daniel
|
|
1998
|
51 |
2 |
p. 288-292
5 p.
|
artikel
|
| 22 |
The Human Lysyl Oxidase-Related Gene (LOXL2) Maps between Markers D8S280 and D8S278 on Chromosome 8p21.2–p21.3
|
Jourdan-Le Saux, Claude
|
|
1998
|
51 |
2 |
p. 305-307
3 p.
|
artikel
|
| 23 |
The Location of HumanCASKat Xp11.4 Identifies This Gene as a Candidate for X-Linked Optic Atrophy
|
Dimitratos, Spiros D.
|
|
1998
|
51 |
2 |
p. 308-309
2 p.
|
artikel
|
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