| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A bone morphogenetic protein subfamily: Chromosomal localization of human genes for BMP5, BMP6, and BMP7
|
Hahn, Gregory V.
|
|
1992
|
14 |
3 |
p. 759-762
4 p.
|
artikel
|
| 2 |
Adult muscle sodium channel α-subunit is a gene candidate for malignant hyperthermia susceptibility
|
Olckers, A.
|
|
1992
|
14 |
3 |
p. 829-831
3 p.
|
artikel
|
| 3 |
A genetic linkage map of human chromosome 9q
|
Ozelius, Laurie J.
|
|
1992
|
14 |
3 |
p. 715-720
6 p.
|
artikel
|
| 4 |
A human dimorphism resulting from loss of an Alu
|
Edwards, Mary C.
|
|
1992
|
14 |
3 |
p. 590-597
8 p.
|
artikel
|
| 5 |
A new method for constructing NotI linking and boundary libraries using a restriction trapper
|
Hayashizaki, Yoshihide
|
|
1992
|
14 |
3 |
p. 733-739
7 p.
|
artikel
|
| 6 |
A radiation hybrid map of the proximal short arm of the human X chromosome spanning incontinentia pigmenti 1 (IP1) translocation breakpoints
|
Gorski, Jerome L.
|
|
1992
|
14 |
3 |
p. 657-665
9 p.
|
artikel
|
| 7 |
A radiation hybrid map of the region on human chromosome 22 containing the neurofibromatosis type 2 locus
|
Frazer, Kelly A.
|
|
1992
|
14 |
3 |
p. 574-584
11 p.
|
artikel
|
| 8 |
Architecture of the canine IDUA gene and mutation underlying canine mucopolysaccharidosis I
|
Menon, Kaushiki P.
|
|
1992
|
14 |
3 |
p. 763-768
6 p.
|
artikel
|
| 9 |
Assignment of a novel protein tyrosine phosphatase gene (Hcph) to mouse chromosome 6
|
Yi, Taolin
|
|
1992
|
14 |
3 |
p. 793-795
3 p.
|
artikel
|
| 10 |
Assignment of the genes encoding human interleukin-8 receptor types 1 and 2 and an interleukin-8 receptor pseudogene to chromosome 2q35
|
Morris, Stephan W.
|
|
1992
|
14 |
3 |
p. 685-691
7 p.
|
artikel
|
| 11 |
Assignment of the human CD30 (Ki-1) gene to 1p36
|
Fonatsch, Christa
|
|
1992
|
14 |
3 |
p. 825-826
2 p.
|
artikel
|
| 12 |
Assignment of the human fas antigen gene (FAS) to 10q24.1
|
Inazawa, Johji
|
|
1992
|
14 |
3 |
p. 821-822
2 p.
|
artikel
|
| 13 |
A testis-expressed Zn finger gene (ZNF76) in human 6p21.3 centromeric to the MHC is closely linked to the human homolog of the t-complex gene tcp-11
|
Ragoussis, Jiannis
|
|
1992
|
14 |
3 |
p. 673-679
7 p.
|
artikel
|
| 14 |
Autosomal dominant retinitis pigmentosa: A novel mutation at the peripherin/RDS locus in the original 6p-linked pedigree
|
Jane Farrar, G.
|
|
1992
|
14 |
3 |
p. 805-807
3 p.
|
artikel
|
| 15 |
Autosomal localization of the amelogenin gene in monotremes and marsupials: Implications for mammalian sex chromosome evolution
|
Watson, Jaclyn M.
|
|
1992
|
14 |
3 |
p. 785-789
5 p.
|
artikel
|
| 16 |
Characterization of three VNTR systems at D21S112
|
Takaesu, Norma
|
|
1992
|
14 |
3 |
p. 816-817
2 p.
|
artikel
|
| 17 |
Chromosomal assignment of 38 human brain expressed sequence tags (ESTs) by analyzing fluorescently labeled PCR products from hybrid cell panels
|
Scott Durkin, A.
|
|
1992
|
14 |
3 |
p. 808-810
3 p.
|
artikel
|
| 18 |
Chromosome 11p15 deletions in human malignant astrocytomas and primitive neuroectodermal tumors
|
Fults, Dan
|
|
1992
|
14 |
3 |
p. 799-801
3 p.
|
artikel
|
| 19 |
Comparison of five tandem repeat loci between humans and chimpanzees
|
Ely, John
|
|
1992
|
14 |
3 |
p. 692-698
7 p.
|
artikel
|
| 20 |
Confirmation of the localization of the human GABAA receptor α1-subunit gene (GABRA1) to distal 5q by linkage analysis
|
Johnson, Keith J.
|
|
1992
|
14 |
3 |
p. 745-748
4 p.
|
artikel
|
| 21 |
Construction and characterization of a region-specific microdissection library from human chromosome 2q35-q37
|
Yu, Jingwei
|
|
1992
|
14 |
3 |
p. 769-774
6 p.
|
artikel
|
| 22 |
Construction of a yeast artificial chromosome contig encompassing the human α5(IV) collagen gene (COL4A5)
|
Vetrie, David
|
|
1992
|
14 |
3 |
p. 634-642
9 p.
|
artikel
|
| 23 |
Dinucleotide repeat (GT) n markers on chromosome 21
|
Warren, Andrew C.
|
|
1992
|
14 |
3 |
p. 818-819
2 p.
|
artikel
|
| 24 |
DNA rearrangements in the α5(IV) collagen gene (COL4A5) of individuals with alport syndrome: Further refinement using pulsed-field gel electrophoresis
|
Vetrie, David
|
|
1992
|
14 |
3 |
p. 624-633
10 p.
|
artikel
|
| 25 |
Duplication/deficiency mapping of situs inversus viscerum (iv), a gene that determines left-right asymmetry in the mouse
|
McGrath, James
|
|
1992
|
14 |
3 |
p. 643-648
6 p.
|
artikel
|
| 26 |
Erratum
|
|
|
1992
|
14 |
3 |
p. 832-
1 p.
|
artikel
|
| 27 |
Evidence for a third transcript from the human factor VIII gene
|
Levinson, Barbara
|
|
1992
|
14 |
3 |
p. 585-589
5 p.
|
artikel
|
| 28 |
Evidence for nonallelic genetic heterogeneity in autosomal recessive retinitis pigmentosa
|
Bleeker-Wagemakers, Liesbeth M.
|
|
1992
|
14 |
3 |
p. 811-812
2 p.
|
artikel
|
| 29 |
Evidence for the localization of a malignant hyperthermia susceptibility locus (MHS2) to human chromosome 17q
|
Levitt, R.C.
|
|
1992
|
14 |
3 |
p. 562-566
5 p.
|
artikel
|
| 30 |
Fine mapping and cloning of the breakpoint associated with menkes syndrome in a female patient
|
Consalez, G. Giacomo
|
|
1992
|
14 |
3 |
p. 557-561
5 p.
|
artikel
|
| 31 |
Fingerprinting human chromosomes by polymerase chain reaction-mediated DNA amplification
|
Sidhu, Mohinderjit S.
|
|
1992
|
14 |
3 |
p. 728-732
5 p.
|
artikel
|
| 32 |
Genetic heterogeneity in X-linked amelogenesis imperfecta
|
Aldred, Michael J.
|
|
1992
|
14 |
3 |
p. 567-573
7 p.
|
artikel
|
| 33 |
Genetic map of nine polymorphic loci comprising a single linkage group on rat chromosome 10: Evidence for linkage conservation with human chromosome 17 and mouse chromosome 11
|
Remmers, Elaine F.
|
|
1992
|
14 |
3 |
p. 618-623
6 p.
|
artikel
|
| 34 |
High-resolution physical mapping of four microsatellite repeat markers near the RYR1 locus on chromosome 19q13.1 and apparent exclusion of the MHS locus from this region in two malignant hyperthermia susceptible families
|
Iles, D.E.
|
|
1992
|
14 |
3 |
p. 749-754
6 p.
|
artikel
|
| 35 |
Identification of a processed pseudogene related to the functional gene encoding the GM2 activator protein: Localization of the pseudogene to human chromosome 3 and the functional gene to human chromosome 5
|
Xie, Bei
|
|
1992
|
14 |
3 |
p. 796-798
3 p.
|
artikel
|
| 36 |
Isolation, mapping, and characterization of two cDNA clones expressed in the cerebellum
|
Eng, Christine M.
|
|
1992
|
14 |
3 |
p. 813-815
3 p.
|
artikel
|
| 37 |
Isolation of DNA markers from a region between incontinentia pigmenti 1 (IP1) X-chromosomal translocation breakpoints by a comparative PCR analysis of a radiation hybrid subclone mapping panel
|
Gorski, Jerome L.
|
|
1992
|
14 |
3 |
p. 649-656
8 p.
|
artikel
|
| 38 |
Linkage analysis demonstrates that the Timp-2 locus is on mouse chromosome 11
|
Stetler-Stevenson, William G.
|
|
1992
|
14 |
3 |
p. 828-829
2 p.
|
artikel
|
| 39 |
Linkage studies of usher syndrome type 1: Exclusion results from the usher syndrome consortium
|
Keats, Bronya J.B.
|
|
1992
|
14 |
3 |
p. 707-714
8 p.
|
artikel
|
| 40 |
Localization of brain nitric oxide synthase (NOS) to human chromosome 12
|
Kishimoto, Jiro
|
|
1992
|
14 |
3 |
p. 802-804
3 p.
|
artikel
|
| 41 |
Localization of the gene encoding the α subunit of human interleukin-5 receptor (IL5RA) to chromosome region 3p24–3p26
|
Isobe, Masaharu
|
|
1992
|
14 |
3 |
p. 755-758
4 p.
|
artikel
|
| 42 |
Localization of the human KRAB finger gene ZNF117 (HPF9) to chromosome 7q11.2
|
Bellefroid, Eric J.
|
|
1992
|
14 |
3 |
p. 780-781
2 p.
|
artikel
|
| 43 |
Mapping Creb-1 to chromosome 1 in the mouse
|
Barton, C. Howard
|
|
1992
|
14 |
3 |
p. 790-792
3 p.
|
artikel
|
| 44 |
Mapping of the mouse Rxr loci encoding nuclear retinoid X receptors RXRα, RXRβ, and RXRγ
|
Hoopes, Charles W.
|
|
1992
|
14 |
3 |
p. 611-617
7 p.
|
artikel
|
| 45 |
Molecular cloning and characterization of the rat liver IL-6 signal transducing molecule, gp130
|
Wang, Yang
|
|
1992
|
14 |
3 |
p. 666-672
7 p.
|
artikel
|
| 46 |
Organization of the gene encoding the human macrophage mannose receptor (mrc1)
|
Kim, Song J.
|
|
1992
|
14 |
3 |
p. 721-727
7 p.
|
artikel
|
| 47 |
PAX1, a member of the paired box-containing class of developmental control genes, is mapped to human chromosome 20p11.2 by in Situ hybridization (ISH and FISH)
|
Schnittger, Susanne
|
|
1992
|
14 |
3 |
p. 740-744
5 p.
|
artikel
|
| 48 |
PCR-based detection of two exonic polymorphisms in the human type VII collagen gene (COL7A1) at 3p21.1
|
Christiano, Angela M.
|
|
1992
|
14 |
3 |
p. 827-828
2 p.
|
artikel
|
| 49 |
Rapid generation of region-specific genomic clones by chromosome microdissection: Isolation of DNA from a region frequently deleted in malignant melanoma
|
Guan, Xin-Yuan
|
|
1992
|
14 |
3 |
p. 680-684
5 p.
|
artikel
|
| 50 |
Regional localization of the highly polymorphic locus D11S533 on the linkage map of human chromosome 11q
|
Litt, Michael
|
|
1992
|
14 |
3 |
p. 820-
1 p.
|
artikel
|
| 51 |
Sublocalization of the gene encoding manganese superoxide dismutase (MnSOD/SOD2) to 6q25 by fluorescence in Situ hybridization and somatic cell hybrid mapping
|
Church, Susan L.
|
|
1992
|
14 |
3 |
p. 823-825
3 p.
|
artikel
|
| 52 |
Subregional mapping of 13 single-copy genes on the long arm of chromosome 12 by fluorescence in Situ hybridization
|
Mathew, Susan
|
|
1992
|
14 |
3 |
p. 775-779
5 p.
|
artikel
|
| 53 |
Syntenic assignments of visual transduction genes in cattle
|
Gallagher Jr., Daniel S.
|
|
1992
|
14 |
3 |
p. 699-706
8 p.
|
artikel
|
| 54 |
Systematic detection of errors in genetic linkage data
|
Lincoln, Stephen E.
|
|
1992
|
14 |
3 |
p. 604-610
7 p.
|
artikel
|
| 55 |
The gene for lysyl oxidase maps to mouse chromosome 18
|
Mock, Beverly A.
|
|
1992
|
14 |
3 |
p. 822-823
2 p.
|
artikel
|
| 56 |
The gene for tissue inhibitor of metalloproteinases-2 is localized on human chromosome arm 17q25
|
De Clerck, Yves
|
|
1992
|
14 |
3 |
p. 782-784
3 p.
|
artikel
|
| 57 |
The hypervariable DXS255 locus contains a LINE-1 repetitive element with a CpG island that is extensively methylated only on the active X chromosome
|
Hendriks, Rudolf W.
|
|
1992
|
14 |
3 |
p. 598-603
6 p.
|
artikel
|
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