| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('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.
|
artikel
|
| 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.
|
artikel
|
| 3 |
A linkage map spanning the locus for diastrophic dysplasia (DTD)
|
Hästbacka, Johanna
|
|
1991
|
11 |
4 |
p. 968-973
6 p.
|
artikel
|
| 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.
|
artikel
|
| 5 |
Assignment of human pancreatic lipase gene (PNLIP) to chromosome 10q24–q26
|
Davis, Richard C.
|
|
1991
|
11 |
4 |
p. 1164-1166
3 p.
|
artikel
|
| 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.
|
artikel
|
| 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.
|
artikel
|
| 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.
|
artikel
|
| 9 |
Author index for volume 11
|
|
|
1991
|
11 |
4 |
p. 1176-1179
4 p.
|
artikel
|
| 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.
|
artikel
|
| 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.
|
artikel
|
| 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.
|
artikel
|
| 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.
|
artikel
|
| 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.
|
artikel
|
| 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.
|
artikel
|
| 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.
|
artikel
|
| 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.
|
artikel
|
| 18 |
Chronic multifocal osteomyelitis, a new recessive mutation on Chromosome 18 of the mouse
|
Byrd, Linda
|
|
1991
|
11 |
4 |
p. 794-798
5 p.
|
artikel
|
| 19 |
Construction and characterization of plasmid libraries enriched in sequences from single human chromosomes
|
Collins, Colin
|
|
1991
|
11 |
4 |
p. 997-1006
10 p.
|
artikel
|
| 20 |
Cumulative subject index volumes 9–11
|
|
|
1991
|
11 |
4 |
p. 1180-1213
34 p.
|
artikel
|
| 21 |
D12S17 (YNH15) and D12S25 (CRI-L809) are the same polymorphic locus
|
Ryynänen, Markku
|
|
1991
|
11 |
4 |
p. 1170-
1 p.
|
artikel
|
| 22 |
Erratum
|
|
|
1991
|
11 |
4 |
p. 1174-1175
2 p.
|
artikel
|
| 23 |
Estimation of genetic distances between “reeler” and nearby loci on mouse chromosome 5
|
Dernoncourt, C.
|
|
1991
|
11 |
4 |
p. 1167-1169
3 p.
|
artikel
|
| 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.
|
artikel
|
| 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.
|
artikel
|
| 26 |
Genetic and physical mapping around the properdin P gene
|
Coleman, M.P.
|
|
1991
|
11 |
4 |
p. 991-996
6 p.
|
artikel
|
| 27 |
Genome mapping with anchored clones: Theoretical aspects
|
Ewens, W.J.
|
|
1991
|
11 |
4 |
p. 799-805
7 p.
|
artikel
|
| 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.
|
artikel
|
| 29 |
Genomic mapping by anchoring random clones: A mathematical analysis
|
Arratia, Richard
|
|
1991
|
11 |
4 |
p. 806-827
22 p.
|
artikel
|
| 30 |
Genomic organization and chromosomal localization of the human CTP synthetase gene (CTPS)
|
Yamauchi, Masatake
|
|
1991
|
11 |
4 |
p. 1088-1096
9 p.
|
artikel
|
| 31 |
Genomic organization of the human erythropoietin receptor gene
|
Penny, Laura A.
|
|
1991
|
11 |
4 |
p. 974-980
7 p.
|
artikel
|
| 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.
|
artikel
|
| 33 |
Inactivation of the Rps4 gene on the mouse X chromosome
|
Zinn, Andrew R.
|
|
1991
|
11 |
4 |
p. 1097-1101
5 p.
|
artikel
|
| 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.
|
artikel
|
| 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.
|
artikel
|
| 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.
|
artikel
|
| 37 |
Linkage mapping of human polymorphic proteins identified by two-dimensional electrophoresis
|
Goldman, David
|
|
1991
|
11 |
4 |
p. 875-884
10 p.
|
artikel
|
| 38 |
Linkage of plasminogen (PLG) and apolipoprotein(a) (LPA) in baboons
|
VandeBerg, John L.
|
|
1991
|
11 |
4 |
p. 925-930
6 p.
|
artikel
|
| 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.
|
artikel
|
| 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.
|
artikel
|
| 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.
|
artikel
|
| 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.
|
artikel
|
| 43 |
Mammalian hexokinase 1: Evolutionary conservation and structure to function analysis
|
Griffin, L.D.
|
|
1991
|
11 |
4 |
p. 1014-1024
11 p.
|
artikel
|
| 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.
|
artikel
|
| 45 |
Molecular cloning, chromosomal assignment, and nucleotide sequence of the feline homeobox HOX3A
|
Masuda, Ryuichi
|
|
1991
|
11 |
4 |
p. 1007-1013
7 p.
|
artikel
|
| 46 |
Molecular mapping of the mouse ob mutation
|
Friedman, J.M.
|
|
1991
|
11 |
4 |
p. 1054-1062
9 p.
|
artikel
|
| 47 |
Mouse proacrosin gene: Nucleotide sequence, diploid expression, and chromosomal localization
|
Kremling, Hannelore
|
|
1991
|
11 |
4 |
p. 828-834
7 p.
|
artikel
|
| 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.
|
artikel
|
| 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.
|
artikel
|
| 50 |
Rat hypoxanthine phosphoribosyltransferase cDNA cloning and sequence analysis
|
Chiaverotti, Teresa A.
|
|
1991
|
11 |
4 |
p. 1158-1160
3 p.
|
artikel
|
| 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.
|
artikel
|
| 52 |
Structural analysis of the gene encoding rat uricase
|
Ito, Masaki
|
|
1991
|
11 |
4 |
p. 905-913
9 p.
|
artikel
|
| 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.
|
artikel
|
| 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.
|
artikel
|
| 55 |
Yeast artificial chromosome-based genome mapping: Some lessons from Xq24–q28
|
Schlessinger, David
|
|
1991
|
11 |
4 |
p. 783-793
11 p.
|
artikel
|
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