| no |
title |
author |
magazine |
year |
volume |
issue |
page(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.
|
article
|
| 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.
|
article
|
| 3 |
A new multisequence family in human
|
Assum, Günter
|
|
1991
|
11 |
2 |
p. 397-409
13 p.
|
article
|
| 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.
|
article
|
| 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.
|
article
|
| 6 |
Assignment of the human Ki-67 gene (MKI67)to 10q25-qter
|
Fonatsch, Christa
|
|
1991
|
11 |
2 |
p. 476-477
2 p.
|
article
|
| 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.
|
article
|
| 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.
|
article
|
| 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.
|
article
|
| 10 |
Chromosome mapping of the murine syndecan gene
|
Oettinger, Henry F.
|
|
1991
|
11 |
2 |
p. 334-338
5 p.
|
article
|
| 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.
|
article
|
| 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.
|
article
|
| 13 |
Erratum
|
|
|
1991
|
11 |
2 |
p. 499-
1 p.
|
article
|
| 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.
|
article
|
| 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.
|
article
|
| 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.
|
article
|
| 17 |
Hybridization methods for DNA sequencing
|
Bains, William
|
|
1991
|
11 |
2 |
p. 294-301
8 p.
|
article
|
| 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.
|
article
|
| 19 |
Localization of the fibrillin (FBN) gene to chromosome 15, band q21.1
|
Magenis, R.Ellen
|
|
1991
|
11 |
2 |
p. 346-351
6 p.
|
article
|
| 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.
|
article
|
| 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.
|
article
|
| 22 |
Mapping genes encoding drug-metabolizing enzymes in recombinant inbred mice
|
Miles, John S.
|
|
1991
|
11 |
2 |
p. 309-316
8 p.
|
article
|
| 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.
|
article
|
| 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.
|
article
|
| 25 |
Molecular heterogeneity of β-thalassemia in Mestizo Mexicans
|
Economou, Effrosini P.
|
|
1991
|
11 |
2 |
p. 474-
1 p.
|
article
|
| 26 |
Molecular structure and functional testing of human L1CAM: An interspecies comparison
|
Hlavin, Mary Louise
|
|
1991
|
11 |
2 |
p. 416-423
8 p.
|
article
|
| 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.
|
article
|
| 28 |
Pax: A murine multigene family of paired box-containing genes
|
Walther, Claudia
|
|
1991
|
11 |
2 |
p. 424-434
11 p.
|
article
|
| 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.
|
article
|
| 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.
|
article
|
| 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.
|
article
|
| 32 |
Polymorphisms in the transcribed 3′ untranslated region of eukaryotic genes
|
Levitt, Roy C.
|
|
1991
|
11 |
2 |
p. 484-489
6 p.
|
article
|
| 33 |
Pro-347-Arg mutation of the rhodopsin gene in autosomal dominant retinitis pigmentosa
|
Gal, Andreas
|
|
1991
|
11 |
2 |
p. 468-470
3 p.
|
article
|
| 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.
|
article
|
| 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.
|
article
|
| 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.
|
article
|
| 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.
|
article
|
| 38 |
The cloned butyrylcholinesterase (BCHE) gene maps to a single chromosome site, 3q26
|
Allderdice, P.W.
|
|
1991
|
11 |
2 |
p. 452-454
3 p.
|
article
|
| 39 |
The distal region of 11p13 and associated genetic diseases
|
Mannens, M.
|
|
1991
|
11 |
2 |
p. 284-293
10 p.
|
article
|
| 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.
|
article
|
| 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.
|
article
|
| 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.
|
article
|
| 43 |
The human ICAM2 gene maps to 17q23–25
|
Sansom, David
|
|
1991
|
11 |
2 |
p. 462-464
3 p.
|
article
|
| 44 |
The study of variation in the human genome
|
Bowcock, Anne
|
|
1991
|
11 |
2 |
p. 491-498
8 p.
|
article
|
Journal description