| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A Novel Tandem Repeat Sequence Located on Human Chromosome 4p: Isolation and Characterization
|
Kogi, Mieko
|
|
1997
|
42 |
2 |
p. 278-283
6 p.
|
artikel
|
| 2 |
Avian and Murine LR8B and Human Apolipoprotein E Receptor 2: Differentially Spliced Products from Corresponding Genes
|
Brandes, Christian
|
|
1997
|
42 |
2 |
p. 185-191
7 p.
|
artikel
|
| 3 |
A YAC Contig Joining the Desmocollin and Desmoglein Loci on Human Chromosome 18 and Ordering of the Desmocollin Genes
|
Cowley, Catherine M.E.
|
|
1997
|
42 |
2 |
p. 208-216
9 p.
|
artikel
|
| 4 |
Characterization of HumanSHCp66 cDNA and Its Processed Pseudogene Mapping to Xq12–q13.1
|
Harun, Roslan B.
|
|
1997
|
42 |
2 |
p. 349-352
4 p.
|
artikel
|
| 5 |
Characterization of the Human Gene Encoding the Type Iα and Type Iβ cGMP-Dependent Protein Kinase (PRKG1)
|
ørstavik, Sigurd
|
|
1997
|
42 |
2 |
p. 311-318
8 p.
|
artikel
|
| 6 |
Characterization of the Rhesus Monkey Galactocerebrosidase (GALC) cDNA and Gene and Identification of the Mutation Causing Globoid Cell Leukodystrophy (Krabbe Disease) in This Primate
|
Luzi, Paola
|
|
1997
|
42 |
2 |
p. 319-324
6 p.
|
artikel
|
| 7 |
Cloning of Human Chromosome 17-Specific cDNAs Using Representational Difference Analysis and Human–Mouse Hybrid Cells
|
Tajima, Yasutaka
|
|
1997
|
42 |
2 |
p. 353-355
3 p.
|
artikel
|
| 8 |
Comparison of the Breakpoint Regions of ELE1 and RET Genes Involved in the Generation of RET/PTC3 Oncogene in Sporadic and in Radiation-Associated Papillary Thyroid Carcinomas
|
Bongarzone, Italia
|
|
1997
|
42 |
2 |
p. 252-259
8 p.
|
artikel
|
| 9 |
Construction and Characterization of a Large-Fragment Chicken Bacterial Artificial Chromosome Library
|
Zimmer, Régis
|
|
1997
|
42 |
2 |
p. 217-226
10 p.
|
artikel
|
| 10 |
Detection of Deletion 1154–1156 Hypophosphatasia Mutation Using TNSALP Exon Amplification
|
Orimo, Hideo
|
|
1997
|
42 |
2 |
p. 364-366
3 p.
|
artikel
|
| 11 |
Genomic Organization and Chromosomal Localization of a Member of the MAP Kinase Phosphatase Gene Family to Human Chromosome 11p15.5 and a Pseudogene to 10q11.2
|
Nesbit, M.A.
|
|
1997
|
42 |
2 |
p. 284-294
11 p.
|
artikel
|
| 12 |
Genomic Structure and Chromosomal Localization of the Novel ETS Factor, PE-2 (ERF)
|
de Castro, Carlos M.
|
|
1997
|
42 |
2 |
p. 227-235
9 p.
|
artikel
|
| 13 |
Genomic Structure of the Human Lysosomal α-Mannosidase Gene (MANB)
|
Riise, Hilde Monica Frostad
|
|
1997
|
42 |
2 |
p. 200-207
8 p.
|
artikel
|
| 14 |
Human Cholecystokinin Type A Receptor Gene: Cytogenetic Localization, Physical Mapping, and Identification of Two Missense Variants in Patients with Obesity and Non-Insulin-Dependent Diabetes Mellitus (NIDDM)
|
Inoue, Hiroshi
|
|
1997
|
42 |
2 |
p. 331-335
5 p.
|
artikel
|
| 15 |
Human Dishevelled Genes Constitute a DHR-Containing Multigene Family
|
Semënov, Mikhail V.
|
|
1997
|
42 |
2 |
p. 302-310
9 p.
|
artikel
|
| 16 |
Identification by Shotgun Sequencing, Genomic Organization, and Functional Analysis of a Fourth Arylsulfatase Gene (ARSF) from the Xp22.3 Region
|
Puca, Annibale Alessandro
|
|
1997
|
42 |
2 |
p. 192-199
8 p.
|
artikel
|
| 17 |
Identification, Characterization, and Precise Mapping of a Human Gene Encoding a Novel Membrane-Spanning Protein from the 22q11 Region Deleted in Velo–Cardio–Facial Syndrome
|
Sirotkin, Howard
|
|
1997
|
42 |
2 |
p. 245-251
7 p.
|
artikel
|
| 18 |
Identification of Translocational Breakpoints within the Intron Region before the Last Coding Exon (Exon 12) of theEVI1Gene in Two Cases of CML-BC with Inv(3)(q21q26)
|
Suzukawa, Kazumi
|
|
1997
|
42 |
2 |
p. 356-360
5 p.
|
artikel
|
| 19 |
Identification of Two Novel Isoforms of the ZNF162 Gene: A Growing Family of Signal Transduction and Activator of RNA Proteins
|
Caslini, Corrado
|
|
1997
|
42 |
2 |
p. 268-277
10 p.
|
artikel
|
| 20 |
Mammalian Rh/T2/S-Glycoprotein Ribonuclease Family Genes: Cloning of a Human Member Located in a Region of Chromosome 6 (6q27) Frequently Deleted in Human Malignancies
|
Trubia, M.
|
|
1997
|
42 |
2 |
p. 342-344
3 p.
|
artikel
|
| 21 |
Monoallelic Expression of HumanPEG1/MESTIs Paralleled by Parent-Specific Methylation in Fetuses
|
Riesewijk, Anne M.
|
|
1997
|
42 |
2 |
p. 236-244
9 p.
|
artikel
|
| 22 |
Refined Genetic Location of the Chromosome 2p-Linked Progressive Muscular Dystrophy Gene
|
Illarioshkin, Sergei N.
|
|
1997
|
42 |
2 |
p. 345-348
4 p.
|
artikel
|
| 23 |
Structure of the Human Type I Iodothyronine 5′-Deiodinase Gene and Localization to Chromosome 1p32–p33
|
Jakobs, Tatjana C.
|
|
1997
|
42 |
2 |
p. 361-363
3 p.
|
artikel
|
| 24 |
ThebgAllele Mutation Is Due to a LINE1 Element Retrotransposition
|
Perou, C.M.
|
|
1997
|
42 |
2 |
p. 366-368
3 p.
|
artikel
|
| 25 |
The Human HNP36 Gene Is Localized to Chromosome 11q13 and Produces Alternative Transcripts That Are Not Mutated in Multiple Endocrine Neoplasia, Type 1 (MEN I) Syndrome
|
Williams, John B.
|
|
1997
|
42 |
2 |
p. 325-330
6 p.
|
artikel
|
| 26 |
TheNNP-1Gene (D21S2056E), Which Encodes a Novel Nuclear Protein, Maps in Close Proximity to the Cystatin B Gene within the EPM1 and APECED Critical Region on 21q22.3
|
Jansen, Erik
|
|
1997
|
42 |
2 |
p. 336-341
6 p.
|
artikel
|
| 27 |
The Reticulocalbin Gene Maps to the WAGR Region in Human and to the Small Eye Harwell Deletion in Mouse
|
Kent, Jill
|
|
1997
|
42 |
2 |
p. 260-267
8 p.
|
artikel
|
| 28 |
Transcript Mapping in a 46-kb Sequenced Region at the Core of 12q13.3 Amplification in Human Cancers
|
Elkahloun, Abdel G.
|
|
1997
|
42 |
2 |
p. 295-301
7 p.
|
artikel
|
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