nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A New Locus for Autosomal Recessive Retinitis Pigmentosa (RP19) Maps to 1p13–1p21
|
Martı́nez-Mir, Amalia |
|
1997 |
40 |
1 |
p. 142-146 5 p. |
artikel |
2 |
Assignment of Growth Factor Receptor-Bound Protein 10 (GRB10) to Human Chromosome 7p11.2–p12
|
Jerome, C.A. |
|
1997 |
40 |
1 |
p. 215-216 2 p. |
artikel |
3 |
Assignment of SFA-1 (PETA-3), a Member of the Transmembrane 4 Superfamily, to Human Chromosome 11p15.5 by Fluorescencein SituHybridization
|
Hasegawa, Hitoshi |
|
1997 |
40 |
1 |
p. 193-196 4 p. |
artikel |
4 |
Assignment of the Human Adipocyte Fatty Acid-Binding Protein Gene (FABP4) to Chromosome 8q21 Using Somatic Cell Hybrid and Fluorescencein SituHybridization Techniques
|
Prinsen, Clemens F.M. |
|
1997 |
40 |
1 |
p. 207-209 3 p. |
artikel |
5 |
Assignment of the Human CC Chemokine Gene TARC (SCYA17) to Chromosome 16q13
|
Nomiyama, Hisayuki |
|
1997 |
40 |
1 |
p. 211-213 3 p. |
artikel |
6 |
Assignment of the Human dUTPase Gene (DUT) to Chromosome 15q15–q21.1 by Fluorescencein SituHybridization
|
Cohen, Dana |
|
1997 |
40 |
1 |
p. 213-215 3 p. |
artikel |
7 |
Assignment of the Mouse Ligatin Gene (Lgtn) to Chromosome 1F byin SituHybridization
|
Malnar-Dragojevic, Daniela |
|
1997 |
40 |
1 |
p. 192-193 2 p. |
artikel |
8 |
Astrotactin (ASTN), a Gene for Glial-Guided Neuronal Migration, Maps to Human Chromosome 1q25.2
|
Fink, James M. |
|
1997 |
40 |
1 |
p. 202-205 4 p. |
artikel |
9 |
Backfoot, a Novel Homeobox Gene, Maps to Human Chromosome 5 (BFT) and Mouse Chromosome 13 (Bft)
|
Shang, Jin |
|
1997 |
40 |
1 |
p. 108-113 6 p. |
artikel |
10 |
cDNA Isolation, Expression, and Chromosomal Localization of the Mouse Survival Motor Neuron Gene (Smn)
|
Viollet, Louis |
|
1997 |
40 |
1 |
p. 185-188 4 p. |
artikel |
11 |
Characterization of Glypican-5 and Chromosomal Localization of HumanGPC5,a New Member of the Glypican Gene Family
|
Veugelers, Mark |
|
1997 |
40 |
1 |
p. 24-30 7 p. |
artikel |
12 |
Characterization of the MouseNktrGene and Promoter
|
Simons-Evelyn, Michelle |
|
1997 |
40 |
1 |
p. 94-100 7 p. |
artikel |
13 |
Chromosomal Assignment of 311 Sequences Transcribed in Human Adult Testis
|
Jones, Michael H. |
|
1997 |
40 |
1 |
p. 155-167 13 p. |
artikel |
14 |
Chromosomal Mapping of the Mouse and RatbrtGenes
|
Matsuda, Yoichi |
|
1997 |
40 |
1 |
p. 181-184 4 p. |
artikel |
15 |
Chromosomal Mapping of Two Novel HumanFGFGenes,FGF11andFGF12
|
Verdier, Anne-Sophie |
|
1997 |
40 |
1 |
p. 151-154 4 p. |
artikel |
16 |
Cloning of STRL22, a New Human Gene Encoding a G-Protein-Coupled Receptor Related to Chemokine Receptors and Located on Chromosome 6q27
|
Liao, Fang |
|
1997 |
40 |
1 |
p. 175-180 6 p. |
artikel |
17 |
Construction and Screening of a Cosmid Library Generated from a Somatic Cell Hybrid Bearing Human Chromosome 15
|
McDaniel, Lisa D. |
|
1997 |
40 |
1 |
p. 63-72 10 p. |
artikel |
18 |
Eleven X Chromosome Breakpoints Associated with Premature Ovarian Failure (POF) Map to a 15-Mb YAC Contig Spanning Xq21
|
Sala, Cinzia |
|
1997 |
40 |
1 |
p. 123-131 9 p. |
artikel |
19 |
Fine Chromosome Mapping of the Genes for Human Liver and Muscle Carnitine Palmitoyltransferase I (CPT1A and CPT1B)
|
Britton, Charles H. |
|
1997 |
40 |
1 |
p. 209-211 3 p. |
artikel |
20 |
Framework YAC Contig Anchored into a 3.2-Mb High-Resolution Physical Map in Proximal 11q13
|
Courseaux, Anouk |
|
1997 |
40 |
1 |
p. 13-23 11 p. |
artikel |
21 |
Genes of the Membrane-Type Matrix Metalloproteinase (MT-MMP) Gene Family, MMP14, MMP15, and MMP16, Localize to Human Chromosomes 14, 16, and 8, Respectively
|
Mattei, Marie-Genevieve |
|
1997 |
40 |
1 |
p. 168-169 2 p. |
artikel |
22 |
Genetic Mapping of 21 Genes on Mouse Chromosome 11 Reveals Disruptions in Linkage Conservation with Human Chromosome 5
|
Watkins-Chow, Dawn E. |
|
1997 |
40 |
1 |
p. 114-122 9 p. |
artikel |
23 |
Genetic Mapping of 20 Novel Expressed Sequence Tags from Midgestation Mouse Embryos Suggests Chromosomal Clustering
|
Tchernev, Velizar T. |
|
1997 |
40 |
1 |
p. 170-174 5 p. |
artikel |
24 |
Genomic Organization of the MouseAZ1Gene That Encodes the Protein Localized to Preacrosomes of Spermatids
|
Aoto, Hiroshi |
|
1997 |
40 |
1 |
p. 138-141 4 p. |
artikel |
25 |
Human Fatty Aldehyde Dehydrogenase Gene (ALDH10): Organization and Tissue-Dependent Expression
|
Chang, Cheng |
|
1997 |
40 |
1 |
p. 80-85 6 p. |
artikel |
26 |
Human Neuroserpin (PI12): cDNA Cloning and Chromosomal Localization to 3q26
|
Schrimpf, Sabine P. |
|
1997 |
40 |
1 |
p. 55-62 8 p. |
artikel |
27 |
Identification and Genetic Mapping of a New Polycystic Kidney Disease on Mouse Chromosome 8
|
Janaswami, Poornima M. |
|
1997 |
40 |
1 |
p. 101-107 7 p. |
artikel |
28 |
Identification and Mapping ofCasp7,a Cysteine Protease Resembling CPP32β, Interleukin-1β Converting Enzyme, and CED-3
|
Juan, Todd S.-C. |
|
1997 |
40 |
1 |
p. 86-93 8 p. |
artikel |
29 |
Identification of Novel Exons 3′ to the HumanSNRPNGene
|
Buiting, Karin |
|
1997 |
40 |
1 |
p. 132-137 6 p. |
artikel |
30 |
Localization of the Human CRF2 Receptor to 7p21–p15 by Radiation Hybrid Mapping and FISH Analysis
|
Meyer, Axel H. |
|
1997 |
40 |
1 |
p. 189-190 2 p. |
artikel |
31 |
Mapping, Sequence, and Expression Analysis of the Human Fertilin β Gene (FTNB)
|
Burkin, Heather R. |
|
1997 |
40 |
1 |
p. 190-192 3 p. |
artikel |
32 |
Molecular Cloning of Murine Homologue Dentatorubral-Pallidoluysian Atrophy (DRPLA) cDNA: Strong Conservation of a Polymorphic CAG Repeat in the Murine Gene
|
Oyake, Mutsuo |
|
1997 |
40 |
1 |
p. 205-207 3 p. |
artikel |
33 |
PMM (PMM1), the Human Homologue ofSEC53or Yeast Phosphomannomutase, Is Localized on Chromosome 22q13
|
Matthijs, Gert |
|
1997 |
40 |
1 |
p. 41-47 7 p. |
artikel |
34 |
Structure of the Human Gene Encoding Sterol Regulatory Element Binding Protein 2 (SREBF2)
|
Miserez, André R. |
|
1997 |
40 |
1 |
p. 31-40 10 p. |
artikel |
35 |
TheBmp8Gene Is Expressed in Developing Skeletal Tissue and Maps near theAchondroplasiaLocus on Mouse Chromosome 4
|
DiLeone, Ralph J. |
|
1997 |
40 |
1 |
p. 196-198 3 p. |
artikel |
36 |
The Gene for Pendred Syndrome Is Located between D7S501 and D7S692 in a 1.7-cM Region on Chromosome 7q
|
Coucke, Paul |
|
1997 |
40 |
1 |
p. 48-54 7 p. |
artikel |
37 |
The Genomic Structure of the Gene Defective in Usher Syndrome Type Ib (MYO7A)
|
Kelley, Philip M. |
|
1997 |
40 |
1 |
p. 73-79 7 p. |
artikel |
38 |
The Human HIV-1 Rev Binding-Protein hRIP/Rab (HRB) Maps to Chromosome 2q36
|
Jones, Tania |
|
1997 |
40 |
1 |
p. 198-199 2 p. |
artikel |
39 |
The Limits of Random Fingerprinting
|
Nelson, David O. |
|
1997 |
40 |
1 |
p. 1-12 12 p. |
artikel |
40 |
The Physical and Genetic Map Surrounding theLystGene on Mouse Chromosome 13
|
Misumi, Donald J. |
|
1997 |
40 |
1 |
p. 147-150 4 p. |
artikel |
41 |
The Three Human Trefoil Genes TFF1, TFF2, and TFF3 Are Located within a Region of 55 kb on Chromosome 21q22.3
|
Seib, Thomas |
|
1997 |
40 |
1 |
p. 200-202 3 p. |
artikel |