| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A cluster of CpG islands at D10S94, near the locus responsible for multiple endocrine neoplasia type 2A (MEN2A)
|
Brooks-Wilson, Angela R.
|
|
1992
|
13 |
2 |
p. 339-343
5 p.
|
artikel
|
| 2 |
A genetic linkage map of 96 loci on the short arm of human chromosome 3
|
Tory, Kalman
|
|
1992
|
13 |
2 |
p. 275-286
12 p.
|
artikel
|
| 3 |
A human aldehyde dehydrogenase (Aldose reductase) pseudogene: Nucleotide sequence analysis and assignment to chromosome 3
|
Brown, Linda
|
|
1992
|
13 |
2 |
p. 465-468
4 p.
|
artikel
|
| 4 |
A human moderately repeated Y-specific DNA sequence is evolutionarily conserved in the Y chromosome of the great apes
|
Guttenbach, M.
|
|
1992
|
13 |
2 |
p. 363-367
5 p.
|
artikel
|
| 5 |
A single cyclin A gene and multiple cyclin B1-related sequences are dispersed in the mouse genome
|
Lock, Leslie F.
|
|
1992
|
13 |
2 |
p. 415-424
10 p.
|
artikel
|
| 6 |
Assignment of the gene coding for the α 2-macroglobulin receptor to mouse chromosome 15 and to human chromosome 12q13–q14 by isotopic and nonisotopic in situ hybridization
|
Hilliker, Carl
|
|
1992
|
13 |
2 |
p. 472-474
3 p.
|
artikel
|
| 7 |
Assignment of the homolog of the MAS1 oncogene to mouse chromosome 17
|
Al-Ubaidi, Muayyad R.
|
|
1992
|
13 |
2 |
p. 487-
1 p.
|
artikel
|
| 8 |
Assignment of the human recombination activating gene 1 (RAG1) to the 14q21.3–q22.2 region
|
Blanquet, Véronique
|
|
1992
|
13 |
2 |
p. 488-489
2 p.
|
artikel
|
| 9 |
Baboon apolipoprotein C-I: cDNA and gene structure and evolution
|
Pastorcic, Martine
|
|
1992
|
13 |
2 |
p. 368-374
7 p.
|
artikel
|
| 10 |
Banding profiles of LTR of human endogenous retrovirus HERV-A in 24 chromosomes in somatic cell hybrids
|
Sugino, Hidehiko
|
|
1992
|
13 |
2 |
p. 461-464
4 p.
|
artikel
|
| 11 |
Chromosomal localization in man and rat of the genes encoding the liver-enriched transcription factors C EBP , DBP, and HNF1 LFB-1> (CEBP, DBP, and transcription factor 1, TCF1, respectively) and of the hepatocyte growth factor/scatter factor gene (HGF)
|
Szpirer, Claude
|
|
1992
|
13 |
2 |
p. 293-300
8 p.
|
artikel
|
| 12 |
Chromosomal localization of FLT4, a novel receptor-type tyrosine kinase gene
|
Galland, Franck
|
|
1992
|
13 |
2 |
p. 475-478
4 p.
|
artikel
|
| 13 |
Chromosome 16-specific repetitive DNA sequences that map to chromosomal regions known to undergo breakage/ rearrangement in leukemia cells
|
Stallings, Raymond L.
|
|
1992
|
13 |
2 |
p. 332-338
7 p.
|
artikel
|
| 14 |
Dideoxy fingerprinting (ddF): A rapid and efficient screen for the presence of mutations
|
Sarkar, Gobinda
|
|
1992
|
13 |
2 |
p. 441-443
3 p.
|
artikel
|
| 15 |
Erratum
|
|
|
1992
|
13 |
2 |
p. 493-
1 p.
|
artikel
|
| 16 |
Expression and chromosome localization of the murine cystic fibrosis transmembrane conductance regulator
|
Kelley, Kevin A.
|
|
1992
|
13 |
2 |
p. 381-388
8 p.
|
artikel
|
| 17 |
Fine mapping of the human biglycan (BGN) gene within the Xq28 region employing a hybrid cell panel
|
Traupe, Heiko
|
|
1992
|
13 |
2 |
p. 481-483
3 p.
|
artikel
|
| 18 |
Fluorescence in situ hybridization establishes the order cen-DXS28(C7)-DXS67(B24)-DXS68(L1)-tel in human chromosome Xp21.3
|
Trask, Barbara J.
|
|
1992
|
13 |
2 |
p. 455-457
3 p.
|
artikel
|
| 19 |
Fluorescent in situ identification of human marker chromosomes using flow sorting and Alu element-mediated PCR
|
Suijkerbuijk, Ron F.
|
|
1992
|
13 |
2 |
p. 355-362
8 p.
|
artikel
|
| 20 |
Genetic mapping of four dinucleotide repeat loci, DXS453, DXS458, DXS454, and DXS424, on the X chromosome using multiplex polymerase chain reaction
|
Huang, Tim H.-M.
|
|
1992
|
13 |
2 |
p. 375-380
6 p.
|
artikel
|
| 21 |
Human dopa decarboxylase: Localization to human chromosome 7p11 and characterization of hepatic cDNAs
|
Scherer, Lisa J.
|
|
1992
|
13 |
2 |
p. 469-471
3 p.
|
artikel
|
| 22 |
Human HOX4E: A gene strongly expressed in the adult male and female urogenital tracts
|
Redline, Raymond W.
|
|
1992
|
13 |
2 |
p. 425-430
6 p.
|
artikel
|
| 23 |
Human repeat element-mediated PCR: Cloning and mapping of chromosome 10 DNA markers
|
Brooks-Wilson, Angela R.
|
|
1992
|
13 |
2 |
p. 409-414
6 p.
|
artikel
|
| 24 |
Identification and characterization of a gene at D10S94 in the MEN2A region
|
McDonald, Helen
|
|
1992
|
13 |
2 |
p. 344-348
5 p.
|
artikel
|
| 25 |
Isolation and characterisation of (AC) n microsatellite genetic markers from human chromosome 16
|
Thompson, A.D.
|
|
1992
|
13 |
2 |
p. 402-408
7 p.
|
artikel
|
| 26 |
Linkage mapping of the carbonyl reductase (CBR) gene on human chromosome 21 using a DNA polymorphism in the 3′ untranslated region
|
Avramopoulos, Dimitrios
|
|
1992
|
13 |
2 |
p. 447-448
2 p.
|
artikel
|
| 27 |
Localization of the Mas proto-oncogene to a densely marked region of mouse chromosome 17 associated with genomic imprinting
|
Cebra-Thomas, Judith A.
|
|
1992
|
13 |
2 |
p. 444-446
3 p.
|
artikel
|
| 28 |
Mapping and characterization of a novel human myc-like (MYCLK1) sequence
|
Robertson, Nahid G.
|
|
1992
|
13 |
2 |
p. 449-451
3 p.
|
artikel
|
| 29 |
Mapping of genes for the human C5a receptor (C5AR), human FMLP receptor (FPR), and two FMLP receptor homologue orphan receptors (FPRH1, FPRH2) to chromosome 19
|
Bao, Lu
|
|
1992
|
13 |
2 |
p. 437-440
4 p.
|
artikel
|
| 30 |
Microdissection of human chromosomal regions 8q23.3–q24.11 and 2q33-qter: Construction of DNA libraries and isolation of their clones
|
Hirota, Tetsuya
|
|
1992
|
13 |
2 |
p. 349-354
6 p.
|
artikel
|
| 31 |
Murine chromosomal location of four hepatocyte-enriched transcription factors: HNf-3α, HNF-3β, HNF-3γ, and HNF-4
|
Avraham, Karen B.
|
|
1992
|
13 |
2 |
p. 264-268
5 p.
|
artikel
|
| 32 |
Nonrandom association between huntington disease and two loci separated by about 3 Mb on 4p16.3
|
Andrew, Susan
|
|
1992
|
13 |
2 |
p. 301-311
11 p.
|
artikel
|
| 33 |
Platelet-derived growth factor A chain: Confirmation of localization of PDGFA to chromosome 7p22 and description of an unusual minisatellite
|
Bonthron, David
|
|
1992
|
13 |
2 |
p. 257-263
7 p.
|
artikel
|
| 34 |
Radiation-reduced hybrids for the myotonic dystrophy locus
|
Brook, J.D.
|
|
1992
|
13 |
2 |
p. 243-250
8 p.
|
artikel
|
| 35 |
Rapid isolation of cosmids from defined subregions by differential Alu-PCR hybridization on chromosome 22-specific library
|
Zucman, Jessica
|
|
1992
|
13 |
2 |
p. 395-401
7 p.
|
artikel
|
| 36 |
Refined localization of human connexin32 gene locus, GJB1, to Xq13.1
|
Corcos, Isabel A.
|
|
1992
|
13 |
2 |
p. 479-480
2 p.
|
artikel
|
| 37 |
Regional assignment of the human keratin 5 (KRT5) gene to chromosome 12q near D12S14 by PCR analysis of somatic cell hybrids and multicolor in situ hybridization
|
Bonifas, Jeannette M.
|
|
1992
|
13 |
2 |
p. 452-454
3 p.
|
artikel
|
| 38 |
Related subunits of NF-κB map to two distinct loci associated with translocations in leukemia, NFKB1 and NFKB2
|
Liptay, Susanne
|
|
1992
|
13 |
2 |
p. 287-292
6 p.
|
artikel
|
| 39 |
Small eye (Sey): Cloning and characterization of the murine homolog of the human aniridia gene
|
Ton, Carl C.T.
|
|
1992
|
13 |
2 |
p. 251-256
6 p.
|
artikel
|
| 40 |
Strand-separating conformational polymorphism analysis: Efficacy of detection of point mutations in the human ornithine δ-aminotransferase gene
|
Michaud, Jacques
|
|
1992
|
13 |
2 |
p. 389-394
6 p.
|
artikel
|
| 41 |
Structure and evolution of the human prosaposin chromosomal gene
|
Rorman, Efrat Gavrieli
|
|
1992
|
13 |
2 |
p. 312-318
7 p.
|
artikel
|
| 42 |
The human gene (DSG2) coding for HDGC, a second member of the desmoglein subfamily of the desmosomal cadherins, is, like DSG1 coding for desmoglein DGI, assigned to chromosome 18
|
Arnemann, Joachim
|
|
1992
|
13 |
2 |
p. 484-486
3 p.
|
artikel
|
| 43 |
The human prothymosin α gene family contains several processed pseudogenes lacking deleterious lesions
|
Manrow, Richard E.
|
|
1992
|
13 |
2 |
p. 319-331
13 p.
|
artikel
|
| 44 |
The human THE-LTR(O) and MstII interspersed repeats are subfamilies of a single widely distributed highly variable repeat family
|
Fields, C.A.
|
|
1992
|
13 |
2 |
p. 431-436
6 p.
|
artikel
|
| 45 |
The interferon- and virus-inducible IFI-56K and IFI-54K genes are located on human chromosome 10 at bands q23–q24
|
Lafage, Marina
|
|
1992
|
13 |
2 |
p. 458-460
3 p.
|
artikel
|
| 46 |
The mouse genome project and human genetics
|
Brown, Stephen D.M.
|
|
1992
|
13 |
2 |
p. 490-492
3 p.
|
artikel
|
| 47 |
Uniparental isodisomy due to duplication of chromosome 21 occuring in somatic cells monosomic for chromosome 21
|
Petersen, Michael B.
|
|
1992
|
13 |
2 |
p. 269-274
6 p.
|
artikel
|
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