| no |
title |
author |
magazine |
year |
volume |
issue |
page(s) |
type |
| 1 |
A Complete YAC Contig and Cosmid Interval Map Covering the Entirety of Human Xq21.33 to Xq22.3 from DXS3 to DXS287
|
Kendall, Elaine
|
|
1997
|
43 |
2 |
p. 171-182
12 p.
|
article
|
| 2 |
Assignment of the Human Gene for Smoothelin (SMTN) to Chromosome 22q12 by Fluorescence in Situ Hybridization and Radiation Hybrid Mapping
|
Engelen, J.J.M.
|
|
1997
|
43 |
2 |
p. 245-247
3 p.
|
article
|
| 3 |
Data Note System for Capturing Laboratory Data
|
Graves, Mark
|
|
1997
|
43 |
2 |
p. 232-236
5 p.
|
article
|
| 4 |
Determination of the Genomic Structure of the XNP/ATRX Gene Encoding a Potential Zinc Finger Helicase
|
Villard, Laurent
|
|
1997
|
43 |
2 |
p. 149-155
7 p.
|
article
|
| 5 |
Escape from X Inactivation of Two New Genes Associated with DXS6974E and DXS7020E
|
Esposito, Teresa
|
|
1997
|
43 |
2 |
p. 183-190
8 p.
|
article
|
| 6 |
Evidence of Linkage to 6p23 and Genetic Heterogeneity in Nonsyndromic Cleft Lip with or without Cleft Palate
|
Scapoli, Luca
|
|
1997
|
43 |
2 |
p. 216-220
5 p.
|
article
|
| 7 |
Expression Analysis and Chromosomal Assignment of the HumanSFRS5/SRp40Gene
|
Snow, Bryan E.
|
|
1997
|
43 |
2 |
p. 165-170
6 p.
|
article
|
| 8 |
Genomic Organization and Chromosomal Localization of the Mouse Telencephalin Gene, a Neuronal Member of the ICAM Family
|
Sugino, Hidehiko
|
|
1997
|
43 |
2 |
p. 209-215
7 p.
|
article
|
| 9 |
Genomic Structure and Chromosomal Localization of the Gene Encoding Translin, a Recombination Hotspot Binding Protein
|
Aoki, Katsunori
|
|
1997
|
43 |
2 |
p. 237-241
5 p.
|
article
|
| 10 |
Heterogeneity in Rates of Recombination in the 6-Mb Region Telomeric to the Human Major Histocompatibility Complex
|
Malfroy, L.
|
|
1997
|
43 |
2 |
p. 226-231
6 p.
|
article
|
| 11 |
High-Resolution Recombinational Map of Mouse Chromosome 16
|
Reeves, R.H.
|
|
1997
|
43 |
2 |
p. 202-208
7 p.
|
article
|
| 12 |
Integrated Radiation Hybrid Map of Human Chromosome 2p13: Possible Involvement of Dynactin in Neuromuscular Diseases
|
Korthaus, Dirk
|
|
1997
|
43 |
2 |
p. 242-244
3 p.
|
article
|
| 13 |
Localization of the Gene Encoding the Ran-Binding Protein RanBP2 to Human Chromosome 2q11–q13 by Fluorescencein SituHybridization
|
Krebber, Heike
|
|
1997
|
43 |
2 |
p. 247-248
2 p.
|
article
|
| 14 |
Molecular Characterization of the Gene for Human Cartilage gp-39 (CHI3L1), a Member of the Chitinase Protein Family and Marker for Late Stages of Macrophage Differentiation
|
Rehli, M.
|
|
1997
|
43 |
2 |
p. 221-225
5 p.
|
article
|
| 15 |
Organization of the Human β-Adducin Gene (ADD2)
|
Gilligan, Diana M.
|
|
1997
|
43 |
2 |
p. 141-148
8 p.
|
article
|
| 16 |
Physical and Transcription Map in the Region 14q24.3: Identification of Six Novel Transcripts
|
Roux, Anne-Françoise
|
|
1997
|
43 |
2 |
p. 130-140
11 p.
|
article
|
| 17 |
The Human GeneZFP161on 18p11.21–pter Encodes a Putativec-mycRepressor and Is Homologous to MurineZfp161(Chr 17) andZfp161-rs1(X Chr)
|
Sobek-Klocke, Ingeborg
|
|
1997
|
43 |
2 |
p. 156-164
9 p.
|
article
|
| 18 |
The Human Homogentisate 1,2-Dioxygenase (HGO) Gene
|
Granadino, B.
|
|
1997
|
43 |
2 |
p. 115-122
8 p.
|
article
|
| 19 |
Three Genes Encoding Zinc Finger Proteins on Human Chromosome 6p21.3: Members of a New Subclass of the Krüppel Gene Family Containing the Conserved SCAN Box Domain
|
Lee, Pauline L.
|
|
1997
|
43 |
2 |
p. 191-201
11 p.
|
article
|
| 20 |
Two Distinct Deletions in theIDSGene and the GeneW: A Novel Type of Mutation Associated with the Hunter Syndrome
|
Karsten, Stanislav L.
|
|
1997
|
43 |
2 |
p. 123-129
7 p.
|
article
|
Journal description