| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A Heterozygous Putative Null Mutation in ROM1 without a Mutation in Peripherin/RDS in a Family with Retinitis Pigmentosa
|
Sakuma, Hitoshi
|
|
1995
|
27 |
2 |
p. 384-386
3 p.
|
artikel
|
| 2 |
A Human Homologue of the Drosophila Polarity Gene frizzled Has Been Identified and Mapped to 17q21.1
|
Zhao, Zhaoyang
|
|
1995
|
27 |
2 |
p. 370-373
4 p.
|
artikel
|
| 3 |
Allele-Dependent Recombination Frequency: Homology Requirement in Meiotic Recombination at the Hot Spot in the Mouse Major Histocompatibility Complex
|
Yoshino, Masayasu
|
|
1995
|
27 |
2 |
p. 298-305
8 p.
|
artikel
|
| 4 |
Assignment of Human α-Synuclein (SNCA) and β-Synuclein (SNCB) Genes to Chromosomes 4q21 and 5q35
|
Spillantini, Maria Grazia
|
|
1995
|
27 |
2 |
p. 379-381
3 p.
|
artikel
|
| 5 |
CHUK, a Conserved Helix-Loop-Helix Ubiquitous Kinase, Maps to Human Chromosome 10 and Mouse Chromosome 19
|
Mock, Beverly A.
|
|
1995
|
27 |
2 |
p. 348-351
4 p.
|
artikel
|
| 6 |
Cloning and Chromosomal Localization of the Human A2b Adenosine Receptor Gene (ADORA2B) and Its Pseudogene
|
Jacobson, Marlene A.
|
|
1995
|
27 |
2 |
p. 374-376
3 p.
|
artikel
|
| 7 |
Cloning and Mapping of the U2af1-rs2 Gene with a High Transmission Distortion in Interspecific Backcross Progeny
|
Yamaoka, Tetsuji
|
|
1995
|
27 |
2 |
p. 337-340
4 p.
|
artikel
|
| 8 |
Complete Sequence of the 43-kb Human Ribosomal DNA Repeat: Analysis of the Intergenic Spacer
|
Gonzalez, Iris L.
|
|
1995
|
27 |
2 |
p. 320-328
9 p.
|
artikel
|
| 9 |
Epidermal Surface Antigen (M517S1) Is Highly Conserved between Mouse and Human
|
Cho, Yoon-Jae
|
|
1995
|
27 |
2 |
p. 251-258
8 p.
|
artikel
|
| 10 |
Erratum
|
|
|
1995
|
27 |
2 |
p. 387-
1 p.
|
artikel
|
| 11 |
Genomic Sequences and Structural Organization of the Human Nidogen Gene (NID)
|
Zimmermann, Katrin
|
|
1995
|
27 |
2 |
p. 245-250
6 p.
|
artikel
|
| 12 |
Human Chromosome 17 Comparative Anchor Loci Are Conserved on Bovine Chromosome 19
|
Yang, Ya-Ping
|
|
1995
|
27 |
2 |
p. 293-297
5 p.
|
artikel
|
| 13 |
Human Gene for the Large Subunit of Ribonucleotide Reductase (RRM1): Functional Analysis of the Promoter
|
Parker, Nigel J.
|
|
1995
|
27 |
2 |
p. 280-285
6 p.
|
artikel
|
| 14 |
Human Growth Hormone-Related latrogenic Creutzfeldt-Jakob Disease: Search for a Genetic Susceptibility by Analysis of the PRNP Coding Region
|
Jaegly, Alexandre
|
|
1995
|
27 |
2 |
p. 382-383
2 p.
|
artikel
|
| 15 |
Identification, Expression, and Pharmacology of a Cys23-Ser23 Substitution in the Human 5-HT2C Receptor Gene (HTR2C)
|
Lappalainen, Jaakko
|
|
1995
|
27 |
2 |
p. 274-279
6 p.
|
artikel
|
| 16 |
Isolation and Fine Mapping of 16 Novel Human Zinc Finger-Encoding cDNAs Identify Putative Candidate Genes for Developmental and Malignant Disorders
|
Tommerup, N.
|
|
1995
|
27 |
2 |
p. 259-264
6 p.
|
artikel
|
| 17 |
41 Kilobases of Analyzed Sequence from the Pseudoautosomal and Sex-Determining Regions of the Short Arm of the Human Y Chromosome
|
Whitfield, L.Simon
|
|
1995
|
27 |
2 |
p. 306-311
6 p.
|
artikel
|
| 18 |
Linkage and Candidate Gene Analysis of X-Linked Familial Exudative Vitreoretinopathy
|
Shastry, Barkur S.
|
|
1995
|
27 |
2 |
p. 341-344
4 p.
|
artikel
|
| 19 |
Linkage Disequilibrium Utilized to Establish a Refined Genetic Position of the Salla Disease Locus on 6q14-q15
|
Schleutker, Johanna
|
|
1995
|
27 |
2 |
p. 286-292
7 p.
|
artikel
|
| 20 |
Localization of the Gene (SYM1) for Proximal Symphalangism to Human Chromosome 17q21-q22
|
Polymeropoulos, Mihael H.
|
|
1995
|
27 |
2 |
p. 225-229
5 p.
|
artikel
|
| 21 |
Mapping of Retrotransposon Sequences in the Unstable Region Surrounding the Spinal Muscular Atrophy Locus in 5q13
|
Francis, M.J.
|
|
1995
|
27 |
2 |
p. 366-369
4 p.
|
artikel
|
| 22 |
Mapping of the Gene for the Mel1a-Melatonin Receptor to Human Chromosome 4 (MTNR1A) and Mouse Chromosome 8 (Mtnr1a)
|
Slaugenhaupt, Susan A.
|
|
1995
|
27 |
2 |
p. 355-357
3 p.
|
artikel
|
| 23 |
β-1,4-N-Acetylgalactosaminyltransferase Involved in Ganglioside Synthesis: cDNA Sequence, Expression, and Chromosome Mapping of the Mouse Gene
|
Sango, Kazunori
|
|
1995
|
27 |
2 |
p. 362-365
4 p.
|
artikel
|
| 24 |
Physical Mapping of 30 CA Repeats on Human Chromosome 22
|
Demczuk, S.
|
|
1995
|
27 |
2 |
p. 345-347
3 p.
|
artikel
|
| 25 |
Precise Localization of Aphidicolin-Induced Breakpoints on the Short Arm of Human Chromosome 3
|
Paradee, William
|
|
1995
|
27 |
2 |
p. 358-361
4 p.
|
artikel
|
| 26 |
Relative Efficiencies of χ2 Models of Recombination for Exclusion Mapping and Gene Ordering
|
Goldstein, Darlene R.
|
|
1995
|
27 |
2 |
p. 265-273
9 p.
|
artikel
|
| 27 |
Structural Organization and Mapping of the Human TCF11 Gene
|
Luna, Luisa
|
|
1995
|
27 |
2 |
p. 237-244
8 p.
|
artikel
|
| 28 |
Structural Organization of the Human Gene (LMNB1) Encoding Nuclear Lamin B1
|
Lin, Feng
|
|
1995
|
27 |
2 |
p. 230-236
7 p.
|
artikel
|
| 29 |
Structure and Chromosomal Localization of a Human Water Channel (AQP3) Gene
|
Ishibashi, Kenichi
|
|
1995
|
27 |
2 |
p. 352-354
3 p.
|
artikel
|
| 30 |
Structure and Organization of the Human Thrombospondin 3 Gene (THBS3)
|
Adolph, Kenneth W.
|
|
1995
|
27 |
2 |
p. 329-336
8 p.
|
artikel
|
| 31 |
The Genes for the α-Type HC3 (PMSA2) and β-Type HC5 (PMSB1) Subunits of Human Proteasomes Map to Chromosomes 6q27 and 7p12-p13 by Fluorescence in Situ Hybridization
|
Okumura, Katsuzumi
|
|
1995
|
27 |
2 |
p. 377-379
3 p.
|
artikel
|
| 32 |
The HIP116 SNF2/SW12-Related Transcription Factor Gene (SNF2L3) Is Located on Human Chromosome 3q25.1-q26.1
|
Lin, Ying
|
|
1995
|
27 |
2 |
p. 381-382
2 p.
|
artikel
|
| 33 |
The Structures of the Human Calcium Channel α1 Subunit (CACNL1A2) and β Subunit (CACNLB3) Genes
|
Yamada, Yuichiro
|
|
1995
|
27 |
2 |
p. 312-319
8 p.
|
artikel
|
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