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                             55 results found
no title author magazine year volume issue page(s) type
1 A brain L-type calcium channel α1 subunit gene (CCHL1A2) maps to mouse chromosome 14 and human chromosome 3 Chin, Hemin
1991
11 4 p. 914-919
6 p.
article
2 A gene encoding a fibroblast growth factor receptor isolated from the Huntington disease gene region of human chromosome 4 Thompson, Leslie M.
1991
11 4 p. 1133-1142
10 p.
article
3 A linkage map spanning the locus for diastrophic dysplasia (DTD) Hästbacka, Johanna
1991
11 4 p. 968-973
6 p.
article
4 A multipedigree linkage study of X-linked deafness: Linkage to Xq13-q21 and evidence for genetic heterogeneity Reardon, W.
1991
11 4 p. 885-894
10 p.
article
5 Assignment of human pancreatic lipase gene (PNLIP) to chromosome 10q24–q26 Davis, Richard C.
1991
11 4 p. 1164-1166
3 p.
article
6 Assignment of the gene for cyclic AMP-response element binding protein 2 (CREB2) to human chromosome 2q24.1–q32 Diep, Anh
1991
11 4 p. 1161-1163
3 p.
article
7 Assignment of the human ferrochelatase gene (FECH) and a locus for protoporphyria to chromosome 18q22 Whitcombe, David M.
1991
11 4 p. 1152-1154
3 p.
article
8 Assignment of the human gene for β-microseminoprotein (MSMB) to chromosome 10 and demonstration of related genes in other vertebrates Ulvsbäck, Magnus
1991
11 4 p. 920-924
5 p.
article
9 Author index for volume 11 1991
11 4 p. 1176-1179
4 p.
article
10 Autosomal dominant retinitis pigmentosa: A mutation in codon 178 of the rhodopsin gene in two families of celtic origin Jane Farrar, G.
1991
11 4 p. 1170-1171
2 p.
article
11 Autosomal dominant retinitis pigmentosa: Localization of a disease gene (RP6) to the short arm of chromosome 6 Farrar, G.Jane
1991
11 4 p. 870-874
5 p.
article
12 Bullous pemphigoid antigens (BPAGs): Identification of RFLPs in human BPAG1 and BPAG2, and exclusion as candidate genes in a large kindred with dominant epidermolysis bullosa simplex Ryynänen, Markku
1991
11 4 p. 1025-1029
5 p.
article
13 cDNA cloning of the type 1 neurofibromatosis gene: Complete sequence of the NF1 gene product Marchuk, Douglas A.
1991
11 4 p. 931-940
10 p.
article
14 Characterization and chromosomal mapping of a human steroid 5α-reductase gene and pseudogene and mapping of the mouse homologue Jenkins, Elizabeth P.
1991
11 4 p. 1102-1112
11 p.
article
15 Characterization and functional expression of a cDNA encoding egasyn (esterase-22): the endoplasmic reticulum-targeting protein of β-glucuronidase Ovnic, Mariana
1991
11 4 p. 956-967
12 p.
article
16 Characterization and regional mapping of new anonymous chromosome 20-specific DNA markers isolated from a flow-sorted DNA library Stolz, Frank-Michael
1991
11 4 p. 948-955
8 p.
article
17 Characterization of the human gene for a newly discovered carbonic anhydrase, CA VII, and its localization to chromosome 16 Montgomery, Jeffry C.
1991
11 4 p. 835-848
14 p.
article
18 Chronic multifocal osteomyelitis, a new recessive mutation on Chromosome 18 of the mouse Byrd, Linda
1991
11 4 p. 794-798
5 p.
article
19 Construction and characterization of plasmid libraries enriched in sequences from single human chromosomes Collins, Colin
1991
11 4 p. 997-1006
10 p.
article
20 Cumulative subject index volumes 9–11 1991
11 4 p. 1180-1213
34 p.
article
21 D12S17 (YNH15) and D12S25 (CRI-L809) are the same polymorphic locus Ryynänen, Markku
1991
11 4 p. 1170-
1 p.
article
22 Erratum 1991
11 4 p. 1174-1175
2 p.
article
23 Estimation of genetic distances between “reeler” and nearby loci on mouse chromosome 5 Dernoncourt, C.
1991
11 4 p. 1167-1169
3 p.
article
24 Gene for lymphoid enhancer-binding factor 1 (LEF1) mapped to human chromosome 4 (q23–q25) and mouse chromosome 3 near Egf Milatovich, Athena
1991
11 4 p. 1040-1048
9 p.
article
25 Generation and fluorescent in situ hybridization mapping of yeast artificial chromosomes of 1p, 17p, 17q, and 19q from a hybrid cell line by high-density screening of an amplified library Driesen, M.S.
1991
11 4 p. 1079-1087
9 p.
article
26 Genetic and physical mapping around the properdin P gene Coleman, M.P.
1991
11 4 p. 991-996
6 p.
article
27 Genome mapping with anchored clones: Theoretical aspects Ewens, W.J.
1991
11 4 p. 799-805
7 p.
article
28 Genomic cloning, complete nucleotide sequence, and structure of the human gene encoding the major intrinsic protein (MIP) of the lens Michele Pisano, M.
1991
11 4 p. 981-990
10 p.
article
29 Genomic mapping by anchoring random clones: A mathematical analysis Arratia, Richard
1991
11 4 p. 806-827
22 p.
article
30 Genomic organization and chromosomal localization of the human CTP synthetase gene (CTPS) Yamauchi, Masatake
1991
11 4 p. 1088-1096
9 p.
article
31 Genomic organization of the human erythropoietin receptor gene Penny, Laura A.
1991
11 4 p. 974-980
7 p.
article
32 Identification of multiple CpG islands and associated conserved sequences in a candidate region for the Huntington disease gene Weber, Bernhard
1991
11 4 p. 1113-1124
12 p.
article
33 Inactivation of the Rps4 gene on the mouse X chromosome Zinn, Andrew R.
1991
11 4 p. 1097-1101
5 p.
article
34 Isolation of the human sex determining region from a Y-enriched yeast artificial chromosome library Monaco, Anthony P.
1991
11 4 p. 1049-1053
5 p.
article
35 LINE-1 repetitive DNA probes for species-specific cloning from Mus spretus and Mus domesticus genomes Rikke, Brad A.
1991
11 4 p. 895-904
10 p.
article
36 Linkage mapping of autosomal dominant retinitis pigmentosa (RP1) to the pericentric region of human chromosome 8 Blanton, Susan Halloran
1991
11 4 p. 857-869
13 p.
article
37 Linkage mapping of human polymorphic proteins identified by two-dimensional electrophoresis Goldman, David
1991
11 4 p. 875-884
10 p.
article
38 Linkage of plasminogen (PLG) and apolipoprotein(a) (LPA) in baboons VandeBerg, John L.
1991
11 4 p. 925-930
6 p.
article
39 Localization of a DNA segment encompassing four tRNA genes to human chromosome 14q11 and its use as an anchor locus for linkage analysis Mitchell, Anna
1991
11 4 p. 1063-1070
8 p.
article
40 Localization of the highly polymorphic microsatellite DXS456 on the genetic linkage map of the human X chromosome Fain, Pamela R.
1991
11 4 p. 1155-1157
3 p.
article
41 Localization of the rhabdomyosarcoma t(2;13) breakpoint on a physical map of chromosome 13 Barr, Frederic G.
1991
11 4 p. 941-947
7 p.
article
42 Major rearrangements in the α5(IV) collagen gene in three patients with alport syndrome Boye, Eileen
1991
11 4 p. 1125-1132
8 p.
article
43 Mammalian hexokinase 1: Evolutionary conservation and structure to function analysis Griffin, L.D.
1991
11 4 p. 1014-1024
11 p.
article
44 Mapping HSA 3 loci in cattle: Additional support for the ancestral synteny of HSA 3 and 21 Threadgill, Deborah S.
1991
11 4 p. 1143-1148
6 p.
article
45 Molecular cloning, chromosomal assignment, and nucleotide sequence of the feline homeobox HOX3A Masuda, Ryuichi
1991
11 4 p. 1007-1013
7 p.
article
46 Molecular mapping of the mouse ob mutation Friedman, J.M.
1991
11 4 p. 1054-1062
9 p.
article
47 Mouse proacrosin gene: Nucleotide sequence, diploid expression, and chromosomal localization Kremling, Hannelore
1991
11 4 p. 828-834
7 p.
article
48 Nearly 80% of cystic fibrosis heterozygotes and 64% of couples at risk may be detected through a unique screening of four mutations by ASO reverse dot blot Serre, J.L.
1991
11 4 p. 1149-1151
3 p.
article
49 New strategy for mapping the human genome based on a novel procedure for construction of jumping libraries Zabarovsky, Eugene R.
1991
11 4 p. 1030-1039
10 p.
article
50 Rat hypoxanthine phosphoribosyltransferase cDNA cloning and sequence analysis Chiaverotti, Teresa A.
1991
11 4 p. 1158-1160
3 p.
article
51 Sequence variation between alleles reveals two types of copy correction at the 27-kDa zein locus of maize Das, O.Prem
1991
11 4 p. 849-856
8 p.
article
52 Structural analysis of the gene encoding rat uricase Ito, Masaki
1991
11 4 p. 905-913
9 p.
article
53 The GABAA receptor β3 subunit gene: Characterization of a human cDNA from chromosome 15q11q13 and mapping to a region of conserved synteny on mouse chromosome 7 Wagstaff, J.
1991
11 4 p. 1071-1078
8 p.
article
54 The human T-cell leukemia virus-related endogenous sequence (HRES1) is located on chromosome 1 at q42 Perl, Andras
1991
11 4 p. 1172-1173
2 p.
article
55 Yeast artificial chromosome-based genome mapping: Some lessons from Xq24–q28 Schlessinger, David
1991
11 4 p. 783-793
11 p.
article
                             55 results found
 
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