nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Acknowledgment
|
|
|
1997 |
39 |
1 |
p. 123-125 3 p. |
artikel |
2 |
A Yeast Artificial Chromosome (YAC) Contig Encompassing the Critical Region of the X-Linked Lymphoproliferative Disease (XLP) Locus
|
Lanyi, Arpad |
|
1997 |
39 |
1 |
p. 55-65 11 p. |
artikel |
3 |
Characterization of aMus spretusYAC That Maps to the Pseudoautosomal Region
|
Yen, Chao-Huang |
|
1997 |
39 |
1 |
p. 19-29 11 p. |
artikel |
4 |
Comparative Linkage Mapping of Human Chromosome 13 and Bovine Chromosome 12
|
Sun, H.S. |
|
1997 |
39 |
1 |
p. 47-54 8 p. |
artikel |
5 |
Genomic Cloning and Chromosomal Assignment of the E2F Dimerization PartnerTFDPGene Family
|
Zhang, Yonghui |
|
1997 |
39 |
1 |
p. 95-98 4 p. |
artikel |
6 |
Genomic Structure and Evolution of a Novel Gene (PLA2L) with Duplicated Phospholipase A2-like Domains
|
Kowalski, Paul E. |
|
1997 |
39 |
1 |
p. 38-46 9 p. |
artikel |
7 |
Human Homology and Candidate Genes for theDominant megacolonLocus, a Mouse Model of Hirschsprung Disease
|
Pingault, Véronique |
|
1997 |
39 |
1 |
p. 86-89 4 p. |
artikel |
8 |
Isolation and Regional Mapping of cDNAs Expressed during Early Human Development
|
Jay, Philippe |
|
1997 |
39 |
1 |
p. 104-108 5 p. |
artikel |
9 |
Isolation of a NovelSry-Related Gene That Is Expressed in High-Metastatic K-1735 Murine Melanoma Cells
|
Tani, Masachika |
|
1997 |
39 |
1 |
p. 30-37 8 p. |
artikel |
10 |
Isolation of Novel Genes from the CMT1A Duplication/HNPP Deletion Critical Region in 17p11.2–p12
|
Murakami, Tatsufumi |
|
1997 |
39 |
1 |
p. 99-103 5 p. |
artikel |
11 |
Mapping of a Newly Discovered Human Gene Homologous to the Apoptosis Associated-Murine Mammary Protein, MFG-E8, to Chromosome 15q25
|
Collins, Colin |
|
1997 |
39 |
1 |
p. 117-118 2 p. |
artikel |
12 |
Mapping of the Human Ribosomal Small Subunit Protein Gene RPS24 to the Chromosome 10q22–q23 Boundary
|
Jones, Anne-Marie |
|
1997 |
39 |
1 |
p. 121-122 2 p. |
artikel |
13 |
Mapping of the Ras-GRF2 Gene (GRF2) to Mouse Chromosome 13C3-D1 and Human Chromosome 5q13, near the Ras-GAP Gene
|
Fam, Neil P. |
|
1997 |
39 |
1 |
p. 118-120 3 p. |
artikel |
14 |
Mitogen-InducibleSIPA1Is Mapped to the Conserved Syntenic Groups of Chromosome 19 in Mouse and Chromosome 11q13.3 Centromeric toBCL1in Human
|
Wada, Yasuo |
|
1997 |
39 |
1 |
p. 66-73 8 p. |
artikel |
15 |
Molecular Cloning and Characterization of the Human AE2 Anion Exchanger (SLC4A2) Gene
|
Medina, Juan F. |
|
1997 |
39 |
1 |
p. 74-85 12 p. |
artikel |
16 |
Molecular Cloning and Chromosomal Localization in Human and Mouse of the SH2-Containing Inositol Phosphatase,INPP5D(SHIP)
|
Liu, Q. |
|
1997 |
39 |
1 |
p. 109-112 4 p. |
artikel |
17 |
Molecular Genetic Mapping of the Mouse Male Sterility and Histoincompatibility (mshi) Mutation on Proximal Chromosome 10
|
Turner, Joseph P. |
|
1997 |
39 |
1 |
p. 1-7 7 p. |
artikel |
18 |
The Complete Sequences of the Galago and Rabbit β-Globin Locus Control Regions: Extended Sequence and Functional Conservation Outside the Cores of DNase Hypersensitive Sites
|
Slightom, Jerry L. |
|
1997 |
39 |
1 |
p. 90-94 5 p. |
artikel |
19 |
The Human Inward Rectifying K+Channel Kir 2.2 (KCNJ12) Gene: Gene Structure, Assignment to Chromosome 17p11.1, and Identification of a Simple Tandem Repeat Polymorphism
|
Hugnot, J.P. |
|
1997 |
39 |
1 |
p. 113-116 4 p. |
artikel |
20 |
Wolfram (DIDMOAD) Syndrome and Leber Hereditary Optic Neuropathy (LHON) Are Associated with Distinct Mitochondrial DNA Haplotypes
|
Hofmann, Sabine |
|
1997 |
39 |
1 |
p. 8-18 11 p. |
artikel |