nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Aberrant splicing of phenylalanine hydroxylase mRNA: The major cause for phenylketonuria in parts of southern Europe
|
Dworniczak, B. |
|
1991 |
11 |
2 |
p. 242-246 5 p. |
artikel |
2 |
A deletion map of the human Yq11 region: Implications for the evolution of the Y chromosome and tentative mapping of a locus involved in spermatogenesis
|
Bardoni, Barbara |
|
1991 |
11 |
2 |
p. 443-451 9 p. |
artikel |
3 |
A new multisequence family in human
|
Assum, Günter |
|
1991 |
11 |
2 |
p. 397-409 13 p. |
artikel |
4 |
A physical map of human chromosome 10 and a comparison with an existing genetic map
|
Carson, Nancy L. |
|
1991 |
11 |
2 |
p. 379-388 10 p. |
artikel |
5 |
Assignment of secretogranin I locus to mouse chromosome 2 by in situ hybridization and interspecific backcross analysis
|
Jenkins, Nancy A. |
|
1991 |
11 |
2 |
p. 479-480 2 p. |
artikel |
6 |
Assignment of the human Ki-67 gene (MKI67)to 10q25-qter
|
Fonatsch, Christa |
|
1991 |
11 |
2 |
p. 476-477 2 p. |
artikel |
7 |
Call for a worldwide survey of human genetic diversity: A vanishing opportunity for the Human Genome Project
|
Cavalli-Sforza, L.L. |
|
1991 |
11 |
2 |
p. 490-491 2 p. |
artikel |
8 |
Characterization and mapping of microdissected genomic clones from the adenomatous polyposis coli (APC) region
|
Hampton, Garret |
|
1991 |
11 |
2 |
p. 247-251 5 p. |
artikel |
9 |
Chromosomal localization of a cytochrome b5 gene to human chromosome 18 and a cytochrome b5 pseudogene to the X chromosome
|
Shephard, E.A. |
|
1991 |
11 |
2 |
p. 302-308 7 p. |
artikel |
10 |
Chromosome mapping of the murine syndecan gene
|
Oettinger, Henry F. |
|
1991 |
11 |
2 |
p. 334-338 5 p. |
artikel |
11 |
Cloning of human heparan sulfate proteoglycan core protein, assignment of the gene (HSPG2) to 1p36.1→p35 and identification of a BamHI restriction fragment length polymorphism
|
Kallunki, Pekka |
|
1991 |
11 |
2 |
p. 389-396 8 p. |
artikel |
12 |
Complete nucleotide sequence of the human RCC1 gene involved in coupling between DNA replication and mitosis
|
Furuno, Nobuaki |
|
1991 |
11 |
2 |
p. 459-461 3 p. |
artikel |
13 |
Erratum
|
|
|
1991 |
11 |
2 |
p. 499- 1 p. |
artikel |
14 |
Evolution of the Na,K- and H,K-ATPase β subunit gene family: Structure of the murine Na,K-ATPase β2 subunit gene
|
Shyjan, Andrew W. |
|
1991 |
11 |
2 |
p. 435-442 8 p. |
artikel |
15 |
Fine structure physical mapping of the region of mouse Chromosome 10 homologous to human Chromosome 21
|
MacDonald, Greg |
|
1991 |
11 |
2 |
p. 317-323 7 p. |
artikel |
16 |
Genes on the short arm of the human X chromosome are not shared with the marsupial X
|
Spencer, James A. |
|
1991 |
11 |
2 |
p. 339-345 7 p. |
artikel |
17 |
Hybridization methods for DNA sequencing
|
Bains, William |
|
1991 |
11 |
2 |
p. 294-301 8 p. |
artikel |
18 |
Laser microdissection and single unique primer PCR allow generation of regional chromosome DNA clones from a single human chromosome
|
Hadano, Shinji |
|
1991 |
11 |
2 |
p. 364-373 10 p. |
artikel |
19 |
Localization of the fibrillin (FBN) gene to chromosome 15, band q21.1
|
Magenis, R.Ellen |
|
1991 |
11 |
2 |
p. 346-351 6 p. |
artikel |
20 |
Localization of the human O 6-methylguanine-DNA methyltransferase gene to chromosome 10q24.33-qter
|
Gardner, E. |
|
1991 |
11 |
2 |
p. 475-476 2 p. |
artikel |
21 |
Mapping anti-müllerian hormone (amh) and related sequences in the mouse: Identification of a new region of homology between MMU10 and HSA19p
|
King, Thomas R. |
|
1991 |
11 |
2 |
p. 273-283 11 p. |
artikel |
22 |
Mapping genes encoding drug-metabolizing enzymes in recombinant inbred mice
|
Miles, John S. |
|
1991 |
11 |
2 |
p. 309-316 8 p. |
artikel |
23 |
Mapping of the gene encoding the α subunit of the stimulatory G protein of adenylyl cyclase (GNAS1) to 20q13.2 → q13.3 in human by in situ hybridization
|
Levine, Michael A. |
|
1991 |
11 |
2 |
p. 478-479 2 p. |
artikel |
24 |
Minisatellite “isoallele” discrimination in pseudohomozygotes by single molecule PCR and variant repeat mapping
|
Monckton, Darren G. |
|
1991 |
11 |
2 |
p. 465-467 3 p. |
artikel |
25 |
Molecular heterogeneity of β-thalassemia in Mestizo Mexicans
|
Economou, Effrosini P. |
|
1991 |
11 |
2 |
p. 474- 1 p. |
artikel |
26 |
Molecular structure and functional testing of human L1CAM: An interspecies comparison
|
Hlavin, Mary Louise |
|
1991 |
11 |
2 |
p. 416-423 8 p. |
artikel |
27 |
Mouse minor satellite DNA genetically maps to the centromere and is physically linked to the proximal telomere
|
Kipling, David |
|
1991 |
11 |
2 |
p. 235-241 7 p. |
artikel |
28 |
Pax: A murine multigene family of paired box-containing genes
|
Walther, Claudia |
|
1991 |
11 |
2 |
p. 424-434 11 p. |
artikel |
29 |
PCR amplification of chromosome-specific alpha satellite DNA: Definition of centromeric STS markers and polymorphic analysis
|
Warburton, Peter E. |
|
1991 |
11 |
2 |
p. 324-333 10 p. |
artikel |
30 |
Physical mapping at a potential X-linked retinitis pigmentosa locus (RP3) by pulsed-field gel electrophoresis
|
Musarella, Maria A. |
|
1991 |
11 |
2 |
p. 263-272 10 p. |
artikel |
31 |
Physical mapping of 60 DNA markers in the p21.1 → q21.3 region of the human X chromosome
|
Lafrenière, Ronald G. |
|
1991 |
11 |
2 |
p. 352-363 12 p. |
artikel |
32 |
Polymorphisms in the transcribed 3′ untranslated region of eukaryotic genes
|
Levitt, Roy C. |
|
1991 |
11 |
2 |
p. 484-489 6 p. |
artikel |
33 |
Pro-347-Arg mutation of the rhodopsin gene in autosomal dominant retinitis pigmentosa
|
Gal, Andreas |
|
1991 |
11 |
2 |
p. 468-470 3 p. |
artikel |
34 |
Probe St35-239 (DXYS64) reveals homology between the distal ends of Xq and Yq
|
Pedicini, Antonello |
|
1991 |
11 |
2 |
p. 482-483 2 p. |
artikel |
35 |
Rat gastric H,K-ATPase β-subunit gene: Intron/exon organization, identification of multiple transcription initiation sites, and analysis of the 5′-flanking region
|
Newman, Paul R. |
|
1991 |
11 |
2 |
p. 252-262 11 p. |
artikel |
36 |
Refinement of the localization of human butyrylcholinesterase to chromosome 3q26.1-q26.2 using a PCR-derived probe
|
Gaughan, Glen |
|
1991 |
11 |
2 |
p. 455-458 4 p. |
artikel |
37 |
Regional localization of the hepatocyte growth factor (HGF) gene to human chromosome 7 band q21.1
|
Fukuyama, Ryuichi |
|
1991 |
11 |
2 |
p. 410-415 6 p. |
artikel |
38 |
The cloned butyrylcholinesterase (BCHE) gene maps to a single chromosome site, 3q26
|
Allderdice, P.W. |
|
1991 |
11 |
2 |
p. 452-454 3 p. |
artikel |
39 |
The distal region of 11p13 and associated genetic diseases
|
Mannens, M. |
|
1991 |
11 |
2 |
p. 284-293 10 p. |
artikel |
40 |
The gene encoding human TFE3, a transcription factor that binds the immunoglobulin heavy-chain enhancer, maps to Xp11.22
|
Henthorn, Paula S. |
|
1991 |
11 |
2 |
p. 374-378 5 p. |
artikel |
41 |
The human gene for an epidermal surface antigen (M17S1) is located at 17q11–12
|
Schroeder, Wanda T. |
|
1991 |
11 |
2 |
p. 481-482 2 p. |
artikel |
42 |
The human homolog of the mouse brown gene maps to the short arm of chromosome 9 and extends the known region of homology with mouse chromosome 4
|
Abbott, Cathy |
|
1991 |
11 |
2 |
p. 471-473 3 p. |
artikel |
43 |
The human ICAM2 gene maps to 17q23–25
|
Sansom, David |
|
1991 |
11 |
2 |
p. 462-464 3 p. |
artikel |
44 |
The study of variation in the human genome
|
Bowcock, Anne |
|
1991 |
11 |
2 |
p. 491-498 8 p. |
artikel |