| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A bidirectional YAC walk from the Norrie disease (NDP) locus
|
Black, Graeme C.M.
|
|
1995
|
25 |
3 |
p. 644-649
6 p.
|
artikel
|
| 2 |
A 6-Mb YAC contig in Xp22.1–p22.2 spanning the DXS69E, XE59, GLRA2, PIGA, GRPR, CALB3, and PHKA2 genes
|
Alitalo, Tiina
|
|
1995
|
25 |
3 |
p. 691-700
10 p.
|
artikel
|
| 3 |
Author index for volume 25
|
|
|
1995
|
25 |
3 |
p. 763-766
4 p.
|
artikel
|
| 4 |
Characterization of the human gene for microfibril-associated glycoprotein (MFAP2), assignment to chromosome 1p36.1–p35, and linkage to D1S170
|
Faraco, Juliette
|
|
1995
|
25 |
3 |
p. 630-637
8 p.
|
artikel
|
| 5 |
Chromosomal assignment and genomic structure of Il15
|
Anderson, Dirk M.
|
|
1995
|
25 |
3 |
p. 701-706
6 p.
|
artikel
|
| 6 |
Chromosomal localization of the gastric and brain receptors for cholecystokinin (CCKAR and CCKBR) in human and mouse
|
Huppi, K.
|
|
1995
|
25 |
3 |
p. 727-729
3 p.
|
artikel
|
| 7 |
Chromosomal localization of the γ-glutamyl carboxylase gene at 2p12
|
Kuo, Wen-Lin
|
|
1995
|
25 |
3 |
p. 746-748
3 p.
|
artikel
|
| 8 |
Chromosomal localization of the human prostanoid receptor gene family
|
Duncan, A.M.V.
|
|
1995
|
25 |
3 |
p. 740-742
3 p.
|
artikel
|
| 9 |
Chromosomal mapping of the human smooth muscle actin gene (enteric type, ACTA3) to 2p13.1 and molecular nature of the HindIII polymorphism
|
Ueyama, Hisao
|
|
1995
|
25 |
3 |
p. 720-723
4 p.
|
artikel
|
| 10 |
Cloning and mapping of murine Nfe2l1
|
Mckie, Judith
|
|
1995
|
25 |
3 |
p. 716-719
4 p.
|
artikel
|
| 11 |
COL5a1: fine genetic mapping and exclusion as candidate gene in families with nail-patella syndrome, tuberous sclerosis 1, hereditary hemorrhagic telangiectasia, and Ehlers—Danlos syndrome type II
|
Greenspan, Daniel S.
|
|
1995
|
25 |
3 |
p. 737-739
3 p.
|
artikel
|
| 12 |
Comparative mapping reveals extensive linkage conservation—but with gene order rearrangements—between the pig and the human genomes
|
Johansson, Maria
|
|
1995
|
25 |
3 |
p. 682-690
9 p.
|
artikel
|
| 13 |
Contents of volume 25
|
|
|
1995
|
25 |
3 |
p. III-XII
nvt p.
|
artikel
|
| 14 |
Erratum
|
|
|
1995
|
25 |
3 |
p. 762-
1 p.
|
artikel
|
| 15 |
Evidence for a third genetic locus for autosomal dominant polycystic kidney disease
|
Daoust, Martin C.
|
|
1995
|
25 |
3 |
p. 733-736
4 p.
|
artikel
|
| 16 |
Genetic dissection of susceptibility to radiation-induced apoptosis of thymocytes and mapping of Rapop1, a novel susceptibility gene
|
Mori, Nobuko
|
|
1995
|
25 |
3 |
p. 609-614
6 p.
|
artikel
|
| 17 |
Identification and characterization of a human cDNA homologous to yeast SKI2
|
Lee, Seong-Gene
|
|
1995
|
25 |
3 |
p. 660-666
7 p.
|
artikel
|
| 18 |
Isolation of a YAC clone covering a cluster of nine S100 genes on human chromosome 1q21: rationale for a new nomenclature of the S100 calcium-binding protein family
|
Schäfer, Beat W.
|
|
1995
|
25 |
3 |
p. 638-643
6 p.
|
artikel
|
| 19 |
Localization of short/branched chain Acyl-CoA dehydrogenase (ACADSB) to human chromosome 10
|
Arden, Karen C.
|
|
1995
|
25 |
3 |
p. 743-745
3 p.
|
artikel
|
| 20 |
Localization of the genes for the 100-kDa complement-activating components of Ra-reactive factor (CRARF and Crarf) to human 3q27–q28 and mouse 16B2–B3
|
Takada, Fumio
|
|
1995
|
25 |
3 |
p. 757-759
3 p.
|
artikel
|
| 21 |
Mapping of the HSD17B2 gene encoding type II 17β-hydroxysteroid dehydrogenase close to D16S422 on chromosome 16q24.1–q24.2
|
Durocher, Francine
|
|
1995
|
25 |
3 |
p. 724-726
3 p.
|
artikel
|
| 22 |
Molecular cloning and physical and genetic mapping of a novel human Na+/H+ exchanger (NHE5/SLC9A5) to chromosome 16q22.1
|
Klanke, Charles A.
|
|
1995
|
25 |
3 |
p. 615-622
8 p.
|
artikel
|
| 23 |
Rat karyotyping by fluorescence in situ hybridization (FISH): localization of oncogene c-raf to 4q42, retinoblastoma antioncogene to 15q12, and mitochondrial D-Loop-like sequences to the Y chromosome
|
Zullo, Steve
|
|
1995
|
25 |
3 |
p. 753-756
4 p.
|
artikel
|
| 24 |
Regional localization of the gene for thyroid peroxidase to human chromosome 2p25 and mouse chromosome 12C
|
Endo, Yuichi
|
|
1995
|
25 |
3 |
p. 760-761
2 p.
|
artikel
|
| 25 |
Structural analysis of the 5′ region of mouse and human huntington disease genes reveals conservation of putative promoter region and di- and trinucleotide polymorphisms
|
Lin, Biaoyang
|
|
1995
|
25 |
3 |
p. 707-715
9 p.
|
artikel
|
| 26 |
Structure of the human gene encoding sterol regulatory element binding protein-1 (SREBF1) and localization of SREBF1 and SREBF2 to chromosomes 17p11.2 and 22q13
|
Hua, Xianxin
|
|
1995
|
25 |
3 |
p. 667-673
7 p.
|
artikel
|
| 27 |
The eukaryotic cofactor for the human immunodeficiency virus type 1 (HIV-1) rev protein, eIF-5A, maps to chromosome 17p12–p13: three eIF-5A pseudogenes map to 10q23.3, 17q25, and 19q13.2
|
Steinkasserer, Alexander
|
|
1995
|
25 |
3 |
p. 749-752
4 p.
|
artikel
|
| 28 |
The human gene for neurotrophic tyrosine kinase receptor type 2 (NTRK2) is located on chromosome 9 but is not the familial dysautonomia gene
|
Slaugenhaupt, Susan A.
|
|
1995
|
25 |
3 |
p. 730-732
3 p.
|
artikel
|
| 29 |
The immunoglobulin κ locus of primates
|
Ermert, K.
|
|
1995
|
25 |
3 |
p. 623-629
7 p.
|
artikel
|
| 30 |
The novel gene g17, located in the human major histocompatibility complex, encodes PBX2, a homeodomain-containing protein
|
Aguado, Begoña
|
|
1995
|
25 |
3 |
p. 650-659
10 p.
|
artikel
|
| 31 |
Thermal asymmetric interlaced PCR: automatable amplification and sequencing of insert end fragments from P1 and YAC clones for chromosome walking
|
Liu, Yao-Guang
|
|
1995
|
25 |
3 |
p. 674-681
8 p.
|
artikel
|
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