nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A contig assembly program based on sensitive detection of fragment overlaps
|
Huang, Xiaoqiu |
|
1992 |
14 |
1 |
p. 18-25 8 p. |
artikel |
2 |
A linkage map of mouse chromosome 19: Definition of comparative mapping relationships with human chromosomes 10 and 11 including the MEN1 locus
|
Rochelle, Julie M. |
|
1992 |
14 |
1 |
p. 26-31 6 p. |
artikel |
3 |
A physical map of a 1.3-Mb region on the long arm of chromosome 12, spanning the GLI and LRP loci
|
Forus, Anne |
|
1992 |
14 |
1 |
p. 117-120 4 p. |
artikel |
4 |
Assignment of genes encoding a unique cytokine (IL12) composed of two unrelated subunits to chromosomes 3 and 5
|
Sieburth, D. |
|
1992 |
14 |
1 |
p. 59-62 4 p. |
artikel |
5 |
Characterization of the human kallikrein locus
|
Riegman, P.H.J. |
|
1992 |
14 |
1 |
p. 6-11 6 p. |
artikel |
6 |
Chromosomal assignment of human YAC clones by fluorescence in Situ hybridization: Use of single-yeast-colony PCR and multiple labeling
|
Baldini, Antonio |
|
1992 |
14 |
1 |
p. 181-184 4 p. |
artikel |
7 |
Chromosomal mapping of the human (MACS) and mouse (Macs) genes encoding the MARCKS protein
|
Blackshear, Perry J. |
|
1992 |
14 |
1 |
p. 168-174 7 p. |
artikel |
8 |
Cloning of the human cholesterol 7α-hydroxylase gene (CYP7) and localization to chromosome 8q11–q12
|
Cohen, Jonathan C. |
|
1992 |
14 |
1 |
p. 153-161 9 p. |
artikel |
9 |
Editorial Board
|
|
|
1992 |
14 |
1 |
p. i- 1 p. |
artikel |
10 |
Errata
|
|
|
1992 |
14 |
1 |
p. 208- 1 p. |
artikel |
11 |
Evidence implicating heterozygous deletion of chromosome 7 in the pathogenesis of familial leukemia associated with monosomy 7
|
Shannon, K.M. |
|
1992 |
14 |
1 |
p. 121-125 5 p. |
artikel |
12 |
Evolution of a highly polymorphic human cytochrome P450 gene cluster: CYP2D6
|
Heim, Markus H. |
|
1992 |
14 |
1 |
p. 49-58 10 p. |
artikel |
13 |
Exclusion of chromosome 6 and 8 locations in nonrhodopsin autosomal dominant retinitis pigmentosa families: Further locus heterogeneity in adRP
|
Bashir, R. |
|
1992 |
14 |
1 |
p. 191-193 3 p. |
artikel |
14 |
Fluorescence in Situ hybridization mapping of human chromosome 19: Mapping and verification of cosmid contigs formed by random restriction enzyme fingerprinting
|
Trask, Barbara |
|
1992 |
14 |
1 |
p. 162-167 6 p. |
artikel |
15 |
Generation of 19 STS markers that can be anchored at specific sites on human chromosome 21
|
Tang, Xiaoren |
|
1992 |
14 |
1 |
p. 185-187 3 p. |
artikel |
16 |
Genetic and physical map of the interferon region on chromosome 9p
|
Fountain, Jane W. |
|
1992 |
14 |
1 |
p. 105-112 8 p. |
artikel |
17 |
Homologous chromosomal locations of the four genes for inter-α-inhibitor and pre-α-inhibitor family in human and mouse: Assignment of the ancestral gene for the lipocalin superfamily
|
Salier, J.P. |
|
1992 |
14 |
1 |
p. 83-88 6 p. |
artikel |
18 |
Human chromosome 8 linkage map based on short tandem repeat polymorphisms: Effect of genotyping errors
|
Tomfohrde, James |
|
1992 |
14 |
1 |
p. 144-152 9 p. |
artikel |
19 |
Human DNA polymerase δ gene maps to region 19q13.3–q13.4 by in Situ hybridization
|
Kemper, Robert R. |
|
1992 |
14 |
1 |
p. 205-206 2 p. |
artikel |
20 |
Identification and mapping of six microdissected genomic DNA probes to the proximal region of mouse chromosome 1
|
Vidal, Silvia M. |
|
1992 |
14 |
1 |
p. 32-37 6 p. |
artikel |
21 |
Identification of polymorphic simple sequence repeats in the genome of the zebrafish
|
Goff, Deborah J. |
|
1992 |
14 |
1 |
p. 200-202 3 p. |
artikel |
22 |
Linkage analysis in X-linked congenital stationary night blindness
|
Aldred, M.A. |
|
1992 |
14 |
1 |
p. 99-104 6 p. |
artikel |
23 |
Linkage heterogeneity between the C3 and LDLR and the APOA4 and APOA1 loci in baboons
|
Kammerer, Candace M. |
|
1992 |
14 |
1 |
p. 43-48 6 p. |
artikel |
24 |
Linkage mapping of the human gene for the α 1 subunit of the cardiac DHP-sensitive Ca2+ channel (CACNL1A1) to chromosome 12p13.2-pter using a dinucleotide repeat
|
Powers, Patricia A. |
|
1992 |
14 |
1 |
p. 206-207 2 p. |
artikel |
25 |
Linkage relations between A2M, HOX3, INT1, KRAS2, and PAH on bovine chromosome 5
|
Barendse, William |
|
1992 |
14 |
1 |
p. 38-42 5 p. |
artikel |
26 |
Linkage study of chronic childhood-onset spinal muscular atrophy (SMA): Confirmation of close linkage to D5S39 in French Canadian families
|
Simard, Louise R. |
|
1992 |
14 |
1 |
p. 188-190 3 p. |
artikel |
27 |
Localization of insulin-2 (Ins-2) and the obesity mutant tubby (tub) to distinct regions of mouse chromosome 7
|
Jones, Julie M. |
|
1992 |
14 |
1 |
p. 197-199 3 p. |
artikel |
28 |
Mapping of the regulatory subunits RIβ and RIIβ of cAMP-Dependent protein kinase genes on human chromosome 7
|
Solberg, Rigmor |
|
1992 |
14 |
1 |
p. 63-69 7 p. |
artikel |
29 |
Methylation of the DXS255 hypervariable locus 5′ CCGG site may be affected by factors other than X-chromosome activation status
|
Cachia, P.G. |
|
1992 |
14 |
1 |
p. 70-74 5 p. |
artikel |
30 |
Molecular basis for nonphenylketonuria hyperphenylalaninemia
|
Economou-Petersen, Effrosini |
|
1992 |
14 |
1 |
p. 1-5 5 p. |
artikel |
31 |
Molecular cloning and chromosomal mapping of a cDNA encoding human 80K-L protein: Major substrate for protein kinase C
|
Sakai, Kosuke |
|
1992 |
14 |
1 |
p. 175-178 4 p. |
artikel |
32 |
Organization of the human monoamine oxidase genes and long-range physical mapping around them
|
Chen, Z-Y. |
|
1992 |
14 |
1 |
p. 75-82 8 p. |
artikel |
33 |
Somatic cell mapping, polymorphism, and linkage analysis of bovine prolactin-related proteins and placental lactogen
|
Dietz, Allan B. |
|
1992 |
14 |
1 |
p. 137-143 7 p. |
artikel |
34 |
Synteny mapping in the bovine: Genes from human chromosome 4
|
Zhang, Nan |
|
1992 |
14 |
1 |
p. 131-136 6 p. |
artikel |
35 |
Synteny mapping in the bovine: Genes from human chromosome 5
|
Zhang, Nan |
|
1992 |
14 |
1 |
p. 126-130 5 p. |
artikel |
36 |
The accuracy of DNA sequences: Estimating sequence quality
|
Churchill, Gary A. |
|
1992 |
14 |
1 |
p. 89-98 10 p. |
artikel |
37 |
The CCAAT/enhancer binding protein (C/EBPα) gene (CEBPA) maps to human chromosome 19q13.1 and the related nuclear factor NF-IL6 (C/EBPβ) gene (CEBPB) maps to human chromosome 20q13.1
|
Hendricks-Taylor, L. Ranee |
|
1992 |
14 |
1 |
p. 12-17 6 p. |
artikel |
38 |
The human APO-1 (APT) antigen maps to 10q23, a region that is syntenic with mouse chromosome 19
|
Lichter, Peter |
|
1992 |
14 |
1 |
p. 179-180 2 p. |
artikel |
39 |
The TCF8 gene encoding a zinc finger protein (Nil-2-a) resides on human chromosome 10p11.2
|
Williams, Thomas M. |
|
1992 |
14 |
1 |
p. 194-196 3 p. |
artikel |
40 |
The X-Y homologous gene amelogenin maps to the short arms of both the X and Y chromosomes and is highly conserved in primates
|
Bailey, David M.D. |
|
1992 |
14 |
1 |
p. 203-205 3 p. |
artikel |
41 |
Variations in alphoid DNA sequences escape detection of aneuploidy at interphase by FISH technique
|
Verma, Ram S. |
|
1992 |
14 |
1 |
p. 113-116 4 p. |
artikel |