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                             44 results found
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
                             44 results found
 
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