Digitale Bibliotheek
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                             65 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Analysis of the human cysteine-rich protein gene (CSRP), assignment to chromosome 1q24–1q32, and identification of an associated MspI polymorphism Wang, Xinkang
1992
14 2 p. 391-397
7 p.
artikel
2 A random STS strategy for construction of YAC contigs spanning defined chromosomal regions Cole, Charlotte G.
1992
14 2 p. 256-262
7 p.
artikel
3 Arrangement and localization of the human GM-CSF receptor α chain gene CSF2RA within the X-Y pseudoautosomal region Rappold, Gudrun
1992
14 2 p. 455-461
7 p.
artikel
4 A somatic cell hybrid panel for regional mapping of human chromosome 18 Markie, David
1992
14 2 p. 431-436
6 p.
artikel
5 Assignment, by in Situ hybridization, of the growth arrest-specific gene, Gas-1, to mouse chromosome 13, bands B3–C2 Webb, G.C.
1992
14 2 p. 548-549
2 p.
artikel
6 Assignment of the gene for acetylcholinesterase to distal mouse chromosome 5 Rachinsky, Tara L.
1992
14 2 p. 511-514
4 p.
artikel
7 Assignment of the human gene propionyl coenzyme a carboxylase, α-chain, (PCCA) to chromosome 13q32 by in Situ hybridization Kennerknecht, Ingo
1992
14 2 p. 550-551
2 p.
artikel
8 cDNA surveying of specific tissue expression of human chromosome 19 sequences Dunne, Patrick W.
1992
14 2 p. 263-269
7 p.
artikel
9 Characterization of yeast artificial chromosomes from Plasmodium falciparum: Construction of a stable, representative library and cloning of telomeric DNA fragments Bruin, Derik de
1992
14 2 p. 332-339
8 p.
artikel
10 Chromlook: An interactive program for error detection and mapping in reference linkage data Haines, Jonathan L.
1992
14 2 p. 517-519
3 p.
artikel
11 Chromosomal assignment of a gene encoding a new collagen type (COL15A1) to 9q21 → q22 Huebner, Kay
1992
14 2 p. 220-224
5 p.
artikel
12 Chromosomal localization of the genes encoding the p50/p105 subunits of NF-κB (NFKB2) and the IκB/MAD-3 (NFKBI) inhibitor of NF-κB to 4q24 and 14q13, respectively Le Beau, Michelle M.
1992
14 2 p. 529-531
3 p.
artikel
13 Chromosomal mapping of human cytokeratin 13 gene (KRT13) Romano, V.
1992
14 2 p. 495-497
3 p.
artikel
14 Chromosome jumping from flanking markers defines the minimal region for alf/hsdr-1 within the albino-deletion complex Schedl, Andreas
1992
14 2 p. 288-297
10 p.
artikel
15 Comparative anatomy of the primate major histocompatibility complex DR subregion: Evidence for combinations of DRB genes conserved across species Kasahara, Masanori
1992
14 2 p. 340-349
10 p.
artikel
16 Construction and characterization of a yeast artificial chromosome library containing 1.5 equivalents of human chromosome 21 Potier, M.-C.
1992
14 2 p. 481-483
3 p.
artikel
17 Detailed mapping around the breakpoint of (3;8) translocation in familial renal cell carcinoma and FRA3B Yamakawa, Kazuhiro
1992
14 2 p. 412-416
5 p.
artikel
18 Detection and characterization of “Chimeric” yeast artificial chromosome clones by fluorescent in Situ suppression hybridization Selleri, Licia
1992
14 2 p. 536-541
6 p.
artikel
19 Detection of a polymorphism within the pepsinogen C gene with PCR: Construction of a linkage map around PGC from 6p11–6p21.3 Bowcock, Anne M.
1992
14 2 p. 398-402
5 p.
artikel
20 Detection of single DNA base mutations with mismatch repair enzymes Lu, A-Lien
1992
14 2 p. 249-255
7 p.
artikel
21 Determination of the nucleotide sequence and chromosomal localization of the ATP2B2 Gene Encoding Human Ca2+-Pumping ATPase Isoform PMCA2 Brandt, Paul
1992
14 2 p. 484-487
4 p.
artikel
22 Discrimination between α-satellite DNA sequences from chromosomes 21 and 13 by using polymerase chain reaction Charlieu, Jean-Paul
1992
14 2 p. 515-516
2 p.
artikel
23 DXS89 (pTAK10) detects a homologous sequence on the Y chromosome Hendrickx, Jan
1992
14 2 p. 554-555
2 p.
artikel
24 Exclusion of linkage between hypokalemic periodic paralysis (HOKPP) and three candidate loci Casley, W.L.
1992
14 2 p. 493-494
2 p.
artikel
25 Feline arylsulfatase B (ARSB): Isolation and expression of the cDNA, comparison with human ARSB, and gene localization to feline chromosome A1 Jackson, Christine E.
1992
14 2 p. 403-411
9 p.
artikel
26 Gene order and genetic distance of 13 loci spanning murine chromosome 15 Hameister, H.
1992
14 2 p. 417-422
6 p.
artikel
27 Genetic and physical maps of human chromosome 4 based on dinucleotide repeats Mills, K.A.
1992
14 2 p. 209-219
11 p.
artikel
28 Genetic mapping of tandemly repeated telomeric DNA sequences in tomato (Lycopersicon esculentum) Ganal, Martin W.
1992
14 2 p. 444-448
5 p.
artikel
29 Genetic mapping of the integrin α 1 gene (Vla1) to mouse chromosome 13 Douville, Philippe
1992
14 2 p. 503-505
3 p.
artikel
30 Genomic organization of the human folate receptor genes on chromosome 11q13 Ragoussis, Jiannis
1992
14 2 p. 423-430
8 p.
artikel
31 Highly repeated DNA sequences in birds: The structure and evolution of an abundant, tandemly repeated 190-bp DNA fragment in parrots Madsen, Cort S.
1992
14 2 p. 462-469
8 p.
artikel
32 Identification of three new genes and estimation of the size of the carcinoembryonic antigen family Khan, Wasif Noor
1992
14 2 p. 384-390
7 p.
artikel
33 Length and sequence variation in the apolipoprotein B intron 20 Alu repeat Shriver, Mark D.
1992
14 2 p. 449-454
6 p.
artikel
34 Linkage mapping of the AML1 gene on human chromosome 21 using a DNA polymorphism in the 3′ untranslated region Avramopoulos, Dimitrios
1992
14 2 p. 506-507
2 p.
artikel
35 Localization of the gene encoding RκB (NFRKB), a tissue-specific DNA binding protein, to chromosome 11q24–q25 Adams, Barbara S.
1992
14 2 p. 270-274
5 p.
artikel
36 Localization of the genes for human inositol 1,4,5-trisphosphate 3-kinase A (ITPKA) and B (ITPKB) to chromosome regions 15q14–q21 and 1q41–q43, respectively, by in Situ hybridization Erneux, C.
1992
14 2 p. 546-547
2 p.
artikel
37 Mapping around the Xq13.1 breakpoints of two X/A translocations in hypohidrotic ectodermal dysplasia (EDA) female patients Plougastel, Béatrice
1992
14 2 p. 523-525
3 p.
artikel
38 Mapping human chromosomes by walking with sequence-tagged sites from end fragments of yeast artificial chromosome inserts Kere, Juha
1992
14 2 p. 241-248
8 p.
artikel
39 Mapping human X-linked genes in the phalangerid marsupial Trichosurus vulpecula McKay, Lynne M.
1992
14 2 p. 302-308
7 p.
artikel
40 Mapping of bovine markers CYP21, PRL, and BOLA DRBP1 by genetic linkage analysis in reference pedigrees Creighton, P.
1992
14 2 p. 526-528
3 p.
artikel
41 Mapping of 50 cosmid clones isolated from a flow-sorted human X chromosome library by fluorescence in Situ hybridization Fan, Y.S.
1992
14 2 p. 542-545
4 p.
artikel
42 Mapping of the gene encoding the α-subunit of the human H+, K+-ATPase to chromosome 19q13.1 by fluorescent in Situ hybridization Song, Il
1992
14 2 p. 547-548
2 p.
artikel
43 Mapping of the shortest region of overlap of deletions of the short arm of chromosome 9 associated with human neoplasia Olopade, Olufunmilayo I.
1992
14 2 p. 437-443
7 p.
artikel
44 Mapping of the x-linked form of hyper-IgM syndrome (HIGM1) to Xq26 by close linkage to HPRT Padayachee, M.
1992
14 2 p. 551-553
3 p.
artikel
45 Neural retina-specific leucine zipper gene NRL (D14S46E) maps to human chromosome 14q11.1-q11.2 Yang-Feng, Teresa L.
1992
14 2 p. 491-492
2 p.
artikel
46 Physical and genetic mapping of the telomeric major histocompatibility complex region in man and relevance to the primary hemochromatosis gene (HFE) Gruen, Jeffrey R.
1992
14 2 p. 232-240
9 p.
artikel
47 Physical localization of chromosome 20 markers using somatic cell hybrid cell lines and fluorescence in Situ hybridization Rao, P.N.
1992
14 2 p. 532-535
4 p.
artikel
48 Physical mapping of the albino-deletion complex in the mouse to localize alf/hsdr-1, a locus required for neonatal survival Kelsey, Gavin
1992
14 2 p. 275-287
13 p.
artikel
49 Pig standard bivariate flow karyotype and peak assignment for chromosomes X, Y, 3, and 7 Schmitz, Annette
1992
14 2 p. 357-362
6 p.
artikel
50 Sequence-tagged sites (STSs) for a set of mapped markers on chromosome 21 Tanzi, Rudolph E.
1992
14 2 p. 498-502
5 p.
artikel
51 The defensin-related murine CRS1C gene: Expression in paneth cells and linkage to Defcr, the cryptdin locus Lin, Michael Y.
1992
14 2 p. 363-368
6 p.
artikel
52 The 5′ ends of LINE1 repeats in rabbit DNA define subfamilies and reveal a short sequence conserved between rabbits and humans Price, Douglas K.
1992
14 2 p. 320-331
12 p.
artikel
53 The gene encoding human plasma carboxypeptidase B (CPB2) resides on chromosome 13 Tsai, Siao Ping
1992
14 2 p. 549-550
2 p.
artikel
54 The gene for aarskog syndrome is located between DXS255 and DXS566 (Xp11.2–Xq13) Porteous, M.E.M.
1992
14 2 p. 298-301
4 p.
artikel
55 The gene for a novel epidermal antigen maps near the neurofibromatosis 1 gene Kayes, Lucille M.
1992
14 2 p. 369-376
8 p.
artikel
56 The gene for human transition protein 2: Nucleotide sequence, assignment to the protamine gene cluster, and evidence for its low expression Schlüter, Gregor
1992
14 2 p. 377-383
7 p.
artikel
57 The gene for the cell adhesion molecule m-cadherin maps to mouse chromosome 8 and human chromosome 16q24.1-qter and is near the e-cadherin (uvomorulin) locus in both species Kaupmann, Klemens
1992
14 2 p. 488-490
3 p.
artikel
58 The gene for X-linked hydrocephalus maps to Xq28, distal to DXS52 Lyonnet, Stanislas
1992
14 2 p. 508-510
3 p.
artikel
59 The HRAS1 gene cluster: Two upstream regions recognizing transcripts and a third encoding a gene with a leucine zipper domain Weitzel, Jeffrey N.
1992
14 2 p. 309-319
11 p.
artikel
60 The human galactose-1-phosphate uridyltransferase gene Leslie, Nancy D.
1992
14 2 p. 474-480
7 p.
artikel
61 The human Pi class glutathione transferase sequence at 12q13-q14 is a reverse-transcribed pseudogene Board, P.G.
1992
14 2 p. 470-473
4 p.
artikel
62 The human ubiquitin/52-residue ribosomal protein fusion gene subfamily (UbA52) is composed primarily of processed pseudogenes Baker, Rohan T.
1992
14 2 p. 520-522
3 p.
artikel
63 The mouse α1(XII) and human α1(XII)-like collagen genes are localized on mouse chromosome 9 and human chromosome 6 Oh, Suk P.
1992
14 2 p. 225-231
7 p.
artikel
64 The telomeric 60 kb of chromosome arm 4p is homologous to telomeric regions on 13p, 15p, 21p, and 22p Youngman, Sandra
1992
14 2 p. 350-356
7 p.
artikel
65 Three novel mutations of the ornithine aminotransferase (OAT) gene in gyrate atrophy Park, James K.
1992
14 2 p. 553-554
2 p.
artikel
                             65 gevonden resultaten
 
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