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                             81 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A (CA) n repeat polymorphism for the human skeletal muscle α-actinin gene ACTN2 and its localization on the linkage map of chromosome 1 Beggs, A.H.
 1992
 13 4 p. 1314-1315
2 p.
 artikel
2 A DNA methylation imprint, determined by the sex of the parent, distinguishes the angelman and Prader-Willi syndromes Driscoll, Daniel J.
 1992
 13 4 p. 917-924
8 p.
 artikel
3 A heterozygous 4-bp deletion mutation in the Gsα gene (GNAS1) in a patient with albright hereditary osteodystrophy Weinstein, Lee S.
 1992
 13 4 p. 1319-1321
3 p.
 artikel
4 A high-resolution cytogenetic map of human chromosome 3: Localization of 291 new cosmid markers by direct R-banding fluorescence in situ hybridization Takahashi, Ei-ichi
 1992
 13 4 p. 1047-1055
9 p.
 artikel
5 Alpha satellite DNAs on chromosomes 10 and 12 are both members of the dimeric suprachromosomal subfamily, but display little identity at the nucleotide sequence level Looijenga, L.H.J.
 1992
 13 4 p. 1125-1132
8 p.
 artikel
6 A method for the rapid sequence-independent amplification of microdissected chromosomal material Bohlander, Stefan K.
 1992
 13 4 p. 1322-1324
3 p.
 artikel
7 A molecular genetic linkage map of mouse chromosome 18 reveals extensive linkage conservation with human chromosomes 5 and 18 Justice, Monica J.
 1992
 13 4 p. 1281-1288
8 p.
 artikel
8 A multipoint genetic linkage map of mouse chromosome 18 Johnson, Kenneth R.
 1992
 13 4 p. 1143-1149
7 p.
 artikel
9 Analyzing and comparing nucleic acid sequences by hybridization to arrays of oligonucleotides: Evaluation using experimental models Southern, E.M.
 1992
 13 4 p. 1008-1017
10 p.
 artikel
10 An estimate of the number of genes in the huntington disease gene region and the identification of 13 transcripts in the 4p 16.3 segment Carlock, L.
 1992
 13 4 p. 1108-1118
11 p.
 artikel
11 An interspecific linkage map of mouse chromosome 15 positioned with respect to the centromere Brannan, Camilynn I.
 1992
 13 4 p. 1075-1081
7 p.
 artikel
12 Assignment of a human DNA double-strand break repair gene (XRCC5) to chromosome 2 Chen, David J.
 1992
 13 4 p. 1088-1094
7 p.
 artikel
13 Assignment of the gene coding for hepatocyte growth factor-like protein to mouse chromosome 9 Degen, Sandra J.Friezner
 1992
 13 4 p. 1368-1369
2 p.
 artikel
14 Assignment of the gene encoding the α 1 subunit of the neuroendocrine/brain-type calcium channel (CACNL1A2) to human chromosome 3, band p14.3 Seino, Susumu
 1992
 13 4 p. 1375-1377
3 p.
 artikel
15 Assignment of the human glycogen debrancher gene to chromosome 1p21 Yang-Feng, Teresa L.
 1992
 13 4 p. 931-934
4 p.
 artikel
16 Assignment of the human homologue of the mouse t-complex gene TCTE3 to human chromosome 6q27 Rappold, G.A.
 1992
 13 4 p. 1337-1339
3 p.
 artikel
17 Assignment of the human slow skeletal troponin T gene to 19q13.4 using somatic cell hybrids and fluorescence in situ hybridization analysis Samson, Françoise
 1992
 13 4 p. 1374-1375
2 p.
 artikel
18 Author index for volume 13 1992
 13 4 p. 1385-1389
5 p.
 artikel
19 Automatable screening of yeast artificial-chromosome libraries based on the oligonucleotide-ligation assay Kwok, Pui-Yan
 1992
 13 4 p. 935-941
7 p.
 artikel
20 Base compositional structure of genomes Fickett, James W.
 1992
 13 4 p. 1056-1064
9 p.
 artikel
21 Chromosomal localization of seven neuronal nicotinic acetylcholine receptor subunit genes in humans Anand, René
 1992
 13 4 p. 962-967
6 p.
 artikel
22 Chromosomal localization of three human D5 dopamine receptor genes Grandy, David K.
 1992
 13 4 p. 968-973
6 p.
 artikel
23 Chromosome mapping of the owl monkey CSF1R and IL5 genes Ma, Nancy Shui-Fong
 1992
 13 4 p. 1174-1177
4 p.
 artikel
24 Clustering of C2H2 zinc finger motif sequences within telomeric and fragile site regions of human chromosomes Lichter, Peter
 1992
 13 4 p. 999-1007
9 p.
 artikel
25 Colocalization of the gene for nephrogenic diabetes insipidus (DIR) and the vasopressin type 2 receptor gene (AVPR2) in the Xq28 region van den Ouweland, A.M.W.
 1992
 13 4 p. 1350-1352
3 p.
 artikel
26 Complementary physical and genetic techniques map the vinculin (VCL) gene on chromosome 10q Mulligan, Lois M.
 1992
 13 4 p. 1347-1349
3 p.
 artikel
27 Confirmation of linkage of limb-girdle muscular dystrophy, type 2, to chromosome 15 Young, K.
 1992
 13 4 p. 1370-1371
2 p.
 artikel
28 CpG islands as gene markers in the human genome Larsen, Frank
 1992
 13 4 p. 1095-1107
13 p.
 artikel
29 Deletion mapping of H-Y antigen to the long arm of the human Y chromosome Cantrell, Michael A.
 1992
 13 4 p. 1255-1260
6 p.
 artikel
30 De novo splice site mutation in the antithrombin III (AT3) gene causing recurrent venous thrombosis: Demonstration of exon skipping by ectopic transcript analysis Berg, Lutz-Peter
 1992
 13 4 p. 1359-1361
3 p.
 artikel
31 Determination of the exon structure of the distal portion of the dystrophin gene by vectorette PCR Roberts, Roland G.
 1992
 13 4 p. 942-950
9 p.
 artikel
32 Dissecting (CAC)5 (GTG)5 multilocus fingerprints from man into individual locus-specific, hypervariable components Zischler, Hans
 1992
 13 4 p. 983-990
8 p.
 artikel
33 Dlx2 (Tes1), a homeobox gene of the Distal-less family, assigned to conserved regions on human and mouse chromosomes 2 Özçelik, Tayfun
 1992
 13 4 p. 1157-1161
5 p.
 artikel
34 D21S215 is a (GT) n polymorphic marker close to centromeric alphoid sequences on chromosome 21 Warren, Andrew C.
 1992
 13 4 p. 1365-1367
3 p.
 artikel
35 Eight novel inactivating germ line mutations at the APC gene identified by denaturing gradient gel electrophoresis Fodde, Riccardo
 1992
 13 4 p. 1162-1168
7 p.
 artikel
36 Errata 1992
 13 4 p. 1384-
1 p.
 artikel
37 Evaluation of a cosmid contig physical map of human chromosome 16 Stallings, Raymond L.
 1992
 13 4 p. 1031-1039
9 p.
 artikel
38 Evidence that nucleotide sequence identity is a requirement for meiotic crossing over within the mouse Eb recombinational hot spot Sant'Angelo, Derek B.
 1992
 13 4 p. 1334-1336
3 p.
 artikel
39 Expression of murine cyclin B1 mRNAs and genetic mapping of related genomic sequences Hanley-Hyde, Joan
 1992
 13 4 p. 1018-1030
13 p.
 artikel
40 Extension of the physical map in the region of the mouse X chromosome homologous to human Xq28 and identification of an exception to conserved linkage Faust, Cynthia J.
 1992
 13 4 p. 1289-1295
7 p.
 artikel
41 Fine-mapping of the spinal muscular atrophy locus to a region flanked by MAP1B and D5S6 Brzustowicz, L.M.
 1992
 13 4 p. 991-998
8 p.
 artikel
42 High-resolution cytogenetic-based physical map of human chromosome 16 Callen, D.F.
 1992
 13 4 p. 1178-1185
8 p.
 artikel
43 Human perforin (PRF1) maps to 10q22, a region that is syntenic with mouse chromosome 10 Fink, Thomas M.
 1992
 13 4 p. 1300-1302
3 p.
 artikel
44 Identification and purification of overlapping cosmid clones of the region Xq24-qter of human X chromosome using HPLC Ida, Biunno
 1992
 13 4 p. 1353-1355
3 p.
 artikel
45 Identification of 57 conventional RFLP and 6 VNTR systems with 32 DNA clones on chromosome 11p15 Takita, Ken-ichi
 1992
 13 4 p. 1296-1299
4 p.
 artikel
46 Identification of new markers in Xp21 between DXS28 (C7) and DMD Worley, K.C.
 1992
 13 4 p. 957-961
5 p.
 artikel
47 Identification of two families of satellite-like repetitive DNA sequences from the zebrafish (Brachydanio rerio) Ekker, Marc
 1992
 13 4 p. 1169-1173
5 p.
 artikel
48 In situ mapping of the chicken progesterone receptor gene and the ovalbumin gene Dominguez-Steglich, Marina
 1992
 13 4 p. 1343-1344
2 p.
 artikel
49 In situ mapping of the gene coding for a leucine zipper DNA binding protein (CDR62) to 16p12–16p13.1 Gress, T.
 1992
 13 4 p. 1340-1342
3 p.
 artikel
50 Isolation and mapping of 88 new RFLP markers on human chromosome 8 Emi, Mitsuru
 1992
 13 4 p. 1261-1266
6 p.
 artikel
51 Isolation of a zinc finger motif (ZNF75) mapping on chromosome Xq26 Villa, Anna
 1992
 13 4 p. 1231-1236
6 p.
 artikel
52 Isolation of 1001 new markers from human chromosome 11, excluding the region of 11p13–p15.5, and their sublocalization by a new series of radiation-reduced somatic cell hybrids Gerhard, D.S.
 1992
 13 4 p. 1133-1142
10 p.
 artikel
53 Localization of the human gene for carnitine palmitoyltransferase to 1p13–p11 by nonradioactive in situ hybridization Minoletti, Fabiola
 1992
 13 4 p. 1372-1374
3 p.
 artikel
54 Localization of the human kinesin-related gene to band 10q24 by fluorescence in situ hybridization Tihy, Frédérique
 1992
 13 4 p. 1371-1372
2 p.
 artikel
55 Localization of the t(2;13) breakpoint of alveolar rhabdomyosarcoma on a physical map of chromosome 2 Barr, Frederic G.
 1992
 13 4 p. 1150-1156
7 p.
 artikel
56 Mapping the human acetylcholinesterase gene to chromosome 7q22 by fluorescent in situ hybridization coupled with selective PCR amplification from a somatic hybrid cell panel and chromosome-sorted DNA libraries Ehrlich, Gal
 1992
 13 4 p. 1192-1197
6 p.
 artikel
57 MEPS parameters and graph analysis for the use of recombination to construct ordered sets of overlapping clones Thaler, David S.
 1992
 13 4 p. 1065-1074
10 p.
 artikel
58 Molecular cloning of mouse β 2-glycoprotein I and mapping of the gene to chromosome 11 Nonaka, Mayumi
 1992
 13 4 p. 1082-1087
6 p.
 artikel
59 Multiplex PCR amplification of three microsatellites within the CFTR gene Morral, Núria
 1992
 13 4 p. 1362-1364
3 p.
 artikel
60 NF1-related locus on chromosome 15 Legius, Eric
 1992
 13 4 p. 1316-1318
3 p.
 artikel
61 Nucleotide sequence analysis of 95 kb near the 3′ end of the murine T-cell receptor α δ chain locus: Strategy and methodology Wilson, Richard K.
 1992
 13 4 p. 1198-1208
11 p.
 artikel
62 On the relative importance of marker heterozygosity and intermarker distance in gene mapping Terwilliger, Joseph D.
 1992
 13 4 p. 951-956
6 p.
 artikel
63 Organization, structure, and function of 95 kb of DNA spanning the murine T-cell receptor Cα Cδ region Koop, Ben F.
 1992
 13 4 p. 1209-1230
22 p.
 artikel
64 PCR amplification and analysis of yeast artificial chromosomes Sutcliffe, James S.
 1992
 13 4 p. 1303-1306
4 p.
 artikel
65 Polymorphisms and deduced amino acid substitutions in the coding sequence of the ryanodine receptor (RYR1) gene in individuals with malignant hyperthermia Gillard, Elizabeth F.
 1992
 13 4 p. 1247-1254
8 p.
 artikel
66 11p15.5-Specific libraries for identification of potential gene sequences involved in Beckwith-Wiedemann syndrome and tumorigenesis Puech, A.
 1992
 13 4 p. 1274-1280
7 p.
 artikel
67 Radiation hybrid map spanning the huntington disease gene region of chromosome 4 Altherr, M.R.
 1992
 13 4 p. 1040-1046
7 p.
 artikel
68 Regional localization of three convertases, PC1 (Nec-1), PC2 (Nec-2), and furin (Fur), on mouse chromosomes Copeland, Neal G.
 1992
 13 4 p. 1356-1358
3 p.
 artikel
69 Report on the sequencing by Hybridization workshop Cantor, C.R.
 1992
 13 4 p. 1378-1383
6 p.
 artikel
70 Resolution of the two loci for autosomal dominant aniridia, AN1 and AN2, to a single locus on chromosome 11p13 Lyons, Leslie A.
 1992
 13 4 p. 925-930
6 p.
 artikel
71 Sequence analysis of a full-length cDNA for the murine proα2(I) collagen chain: Comparison of the derived primary structure with human proα2(I) collagen Phillips, Charlotte L.
 1992
 13 4 p. 1345-1346
2 p.
 artikel
72 Sequences from a family of bovine Y-chromosomal repeats Matthews, Margaret E.
 1992
 13 4 p. 1267-1273
7 p.
 artikel
73 Strategy for detecting cellular transcripts promoted by human endogenous long terminal repeats: Identification of a novel gene (CDC4L) with homology to yeast CDC4 Feuchter, Anita E.
 1992
 13 4 p. 1237-1246
10 p.
 artikel
74 Structure and sequence of the human α-l-iduronidase gene Scott, Hamish S.
 1992
 13 4 p. 1311-1313
3 p.
 artikel
75 The amplified long genomic sequence (ALGS) located in the centromeric regions of mouse chromosomes Koide, Tsuyoshi
 1992
 13 4 p. 1186-1191
6 p.
 artikel
76 The evolution of human chromosome 21: Evidence from in situ hybridization in marsupials and a monotreme Maccarone, Pino
 1992
 13 4 p. 1119-1124
6 p.
 artikel
77 The gene encoding the human spasmolytic protein ( SML1 hSP ) is in 21q 22.3, physically linked to the homologous breast cancer marker gene BCEI pS2 Tomasetto, C.
 1992
 13 4 p. 1328-1330
3 p.
 artikel
78 The gene for the dihydropyridine-sensitive calcium channel α2 subunit (CCHL2A) maps to the proximal region of mouse chromosome 5 Chin, Hemin
 1992
 13 4 p. 1325-1327
3 p.
 artikel
79 The genes for MHC class II regulatory factors RFX1 and RFX2 are located on the short arm of chromosome 19 Pugliatti, L.
 1992
 13 4 p. 1307-1310
4 p.
 artikel
80 The human BDNF gene maps between FSHB and HVBS1 at the boundary of 11p13–p14 Hanson, Isabel M.
 1992
 13 4 p. 1331-1333
3 p.
 artikel
81 The mouse CREB (cAMP responsive element binding protein) gene: Structure, promoter analysis, and chromosomal localization Cole, Timothy J.
 1992
 13 4 p. 974-982
9 p.
 artikel
                             81 gevonden resultaten
 
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