Digitale Bibliotheek
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                             43 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A deletion of two nucleotides in exon 10 of the CFTR gene in a Soviet family with cystic fibrosis causing early infant death Ivaschenko, Tatyana E.
1991
10 1 p. 298-299
2 p.
artikel
2 A genetic linkage map of human chromosome 5 with 60 RFLP loci Weiffenbach, Barbara
1991
10 1 p. 173-185
13 p.
artikel
3 A hybrid cell mapping panel for regional localization of probes to human chromosome 8 Wagner, Michael J.
1991
10 1 p. 114-125
12 p.
artikel
4 A linkage map of mouse chromosome 8: Further definition of homologous linkage relationships between mouse chromosome 8 and human chromosomes 8, 16, and 19 Howard, Thad A.
1991
10 1 p. 207-213
7 p.
artikel
5 A new system for high-resolution DNA sequence mapping in interphase pronuclei Brandriff, Brigitte
1991
10 1 p. 75-82
8 p.
artikel
6 Assignment of the human pancreatic colipase gene to chromosome 6p21.1 to pter Davis, Richard C.
1991
10 1 p. 262-265
4 p.
artikel
7 cDNA cloning and chromosomal assignment of the endothelin 2 gene: Vasoactive intestinal contractor peptide is rat endothelin 2 Bloch, Kenneth D.
1991
10 1 p. 236-242
7 p.
artikel
8 Characterization and chromosomal mapping of a genomic clone encoding human alanine:Glyoxylate aminotransferase Purdue, P.Edward
1991
10 1 p. 34-42
9 p.
artikel
9 Characterization of the human argininosuccinate lyase gene and analysis of exon skipping Abramson, Richard D.
1991
10 1 p. 126-132
7 p.
artikel
10 Chromosomal mapping of glutamate dehydrogenase gene sequences to mouse chromosomes 7 and 14 Tzimagiorgis, George
1991
10 1 p. 83-88
6 p.
artikel
11 Complete structure of the human gene encoding neuron-specific enolase Oliva, Daniele
1991
10 1 p. 157-165
9 p.
artikel
12 Deletion mapping of DNA segments from the Y chromosome long arm and their analysis in an XX male Donlon, Timothy A.
1991
10 1 p. 51-56
6 p.
artikel
13 Detection of three rare frameshift mutations in the cystic fibrosis gene in an African-American (CF444delA), an Italian (CF2522insC), and a Soviet (CF3821delT)1 White, Marga Belle
1991
10 1 p. 266-269
4 p.
artikel
14 Erratum 1991
10 1 p. 300-
1 p.
artikel
15 EVX2, a human homeobox gene homologous to the even-skipped segmentation gene, is localized at the 5′ end of HOX4 locus on chromosome 2 D'Esposito, Maurizio
1991
10 1 p. 43-50
8 p.
artikel
16 Genomic DNA sequence of the cystic fibrosis transmembrane conductance regulator (CFTR) gene Zielenski, Julian
1991
10 1 p. 214-228
15 p.
artikel
17 G protein Gsα (GNAS1), the probable candidate gene for albright hereditary osteodystrophy, is assigned to human chromosome 20q12–q13.2 Gopal Rao, V.V.N.
1991
10 1 p. 257-261
5 p.
artikel
18 High-density molecular map of the central span of the mouse X chromosome Brockdorff, N.
1991
10 1 p. 17-22
6 p.
artikel
19 Identification of mutations in exons 1 through 8 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene Zielenski, Julian
1991
10 1 p. 229-235
7 p.
artikel
20 Isolation and regional mapping of NotI and EagI clones from human chromosome 21 Gao, Jizong
1991
10 1 p. 166-172
7 p.
artikel
21 Isolation, characterization, and chromosomal mapping of mouse P450 17α-hydroxylase/C17–20 lyase Youngblood, Geri L.
1991
10 1 p. 270-275
6 p.
artikel
22 Isolation of a variant family of mouse minor satellite DNA that hybridizes preferentially to chromosome 4 Broccoli, Dominique
1991
10 1 p. 68-74
7 p.
artikel
23 Linear order of new and established DNA markers around the fragile site at Xq27.3 Hirst, M.C.
1991
10 1 p. 243-249
7 p.
artikel
24 Linkage of amelogenin (Amel) to the distal portion of the mouse X chromosome Chapman, Verne M.
1991
10 1 p. 23-28
6 p.
artikel
25 Localization of CYP2F1 by multipoint linkage analysis and pulsed-field gel electrophoresis Bale, Allen E.
1991
10 1 p. 284-286
3 p.
artikel
26 Localization of the gene for the Wiskott-Aldrich syndrome between two flanking markers, TIMP and DXS255, on Xp11.22–Xp11.3 Kwan, Sau-Ping
1991
10 1 p. 29-33
5 p.
artikel
27 Mapping nonisotopically labeled DNA probes to human chromosome bands by confocal microscopy Albertson, Donna G.
1991
10 1 p. 143-150
8 p.
artikel
28 Microdeletions within 22q11 associated with sporadic and familial DiGeorge syndrome Scambler, Peter J.
1991
10 1 p. 201-206
6 p.
artikel
29 Molecular characterization of a deletion encompassing the splotch mutation on mouse chromosome 1 Epstein, Douglas J.
1991
10 1 p. 89-93
5 p.
artikel
30 Molecular characterization of rat multigene family encoding proline-rich proteins Lin, Her H.
1991
10 1 p. 102-113
12 p.
artikel
31 Nonhomologous recombination in the human genome: Deletions in the human factor VIII gene Woods-Samuels, Patricia
1991
10 1 p. 94-101
8 p.
artikel
32 Ornithine aminotransferase-related sequences map to two nonadjacent intervals on the human X chromosome short arm Lafreniere, Ronald G.
1991
10 1 p. 276-279
4 p.
artikel
33 Parental origin of chromosome 22 loss in sporadic and NF2 neuromas Fontaine, Bertrand
1991
10 1 p. 280-283
4 p.
artikel
34 Polyamines eliminate an extreme size bias against transformation of large yeast artificial chromosome DNA Connelly, Carla
1991
10 1 p. 10-16
7 p.
artikel
35 Sequences of junction fragments in the deletion-prone region of the dystrophin gene Love, D.R.
1991
10 1 p. 57-67
11 p.
artikel
36 Smallest region of overlap in Wilms tumor deletions uniquely implicates an 11p13 zinc finger gene as the disease locus Ton, Carl C.T.
1991
10 1 p. 293-297
5 p.
artikel
37 Structural organization and complete sequence of the human α-N-acetylgalactosaminidase gene: Homology with the α-galactosidase A gene provides evidence for evolution from a common ancestral gene Wang, Anne M.
1991
10 1 p. 133-142
10 p.
artikel
38 Structure of the human cytochrome c oxidase subunit Vb gene and chromosomal mapping of the coding gene and of seven pseudogenes Lomax, Margaret I.
1991
10 1 p. 1-9
9 p.
artikel
39 Structure of the murine c-sis proto-oncogene (Sis, PDGFB) encoding the B chain of platelet-derived growth factor Bonthron, David T.
1991
10 1 p. 287-292
6 p.
artikel
40 The gene for SP-40,40, human homolog of rat sulfated glycoprotein 2, rat clusterin, and rat testosterone-repressed prostate message 2, maps to chromosome 8 Purrello, Michele
1991
10 1 p. 151-156
6 p.
artikel
41 The human chromosome content in human × rodent somatic cell hybrids analyzed by a screening technique using Alu PCR Bicknell, David C.
1991
10 1 p. 186-192
7 p.
artikel
42 The human connexin gene family of gap junction proteins: Distinct chromosomal locations but similar structures Fishman, Glenn I.
1991
10 1 p. 250-256
7 p.
artikel
43 The search for South European cystic fibrosis mutations: Identification of two new mutations, four variants, and intronic sequences Gasparini, P.
1991
10 1 p. 193-200
8 p.
artikel
                             43 gevonden resultaten
 
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