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                             23 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A long-range restriction map between the α-globin complex and a marker closely linked to the polycystic kidney disease 1 (PKD1) locus Harris, P.C.
1990
7 2 p. 195-206
12 p.
artikel
2 Announcement 1990
7 2 p. 298-
1 p.
artikel
3 A novel human DNA polymorphism resulting from transfer of DNA from chromosome 6 to chromosome 16 Wong, Zilla
1990
7 2 p. 222-234
13 p.
artikel
4 Assignment of the human gene for histidine-rich glycoprotein to chromosome 3 van den Berg, E.A.
1990
7 2 p. 276-279
4 p.
artikel
5 Cloning and characterization of the human β-glucuronidase gene Miller, Raymond D.
1990
7 2 p. 280-283
4 p.
artikel
6 Differential methylation of the hypervariable locus DXS255 on active and inactive X chromosomes correlates with the expression of a human X-linked gene Brown, R.M.
1990
7 2 p. 215-221
7 p.
artikel
7 Human δ-aminolevulinate synthase: Assignment of the housekeeping gene to 3p21 and the erythroid-specific gene to the X chromosome Bishop, David F.
1990
7 2 p. 207-214
8 p.
artikel
8 Human chromosome 17 NotI linking clones and their use in long-range restriction mapping of the Miller-Dieker chromosome region (MDCR) in 17p13.3 Ledbetter, Susan A.
1990
7 2 p. 264-269
6 p.
artikel
9 Human embryonic/atrial myosin alkali light chain gene: Characterization, sequence, and chromosomal location Seharaseyon, Jegatheesan
1990
7 2 p. 289-293
5 p.
artikel
10 Identification of two distinct subfamilies of alpha satellite DNA that are highly specific for human chromosome 15 Choo, K.H.
1990
7 2 p. 143-151
9 p.
artikel
11 Isolation of clones on chromosome 7 that contain recognition sites for rare-cutting enzymes by oligonucleotide hybridization Melmer, Georg
1990
7 2 p. 173-181
9 p.
artikel
12 Localization of the gene encoding a type I protein phosphatase catalytic subunit to human chromosome band 11q13 Barker, Hazel M.
1990
7 2 p. 159-166
8 p.
artikel
13 Localization of the gene for human simple epithelial keratin 18 to chromosome 12 using polymerase chain reaction Waseem, Ahmad
1990
7 2 p. 188-194
7 p.
artikel
14 Localization of Usher syndrome type II to chromosome 1q Kimberling, William J.
1990
7 2 p. 245-249
5 p.
artikel
15 Location of the gene involving the Small eye mutation on mouse chromosome 2 suggests homology with human aniridia 2 (AN2) van der Meer-de Jong, Riet
1990
7 2 p. 270-275
6 p.
artikel
16 Mapping recessive ophthalmic diseases: Linkage of the locus for Usher syndrome type II to a DNA marker on chromosome 1q Lewis, Richard Alan
1990
7 2 p. 250-256
7 p.
artikel
17 Methylation patterns at the hypervariable X-chromosome locus DXS255 (M27β): Correlation with X-inactivation status Boyd, Yvonne
1990
7 2 p. 182-187
6 p.
artikel
18 Multiplex DNA deletion detection and exon sequencing of the hypoxanthine phosphoribosyltransferase gene in Lesch-Nyhan families Gibbs, Richard A.
1990
7 2 p. 235-244
10 p.
artikel
19 Rapid isolation of human chromosome-specific DNA probes from a somatic cell hybrid Cotter, Finbarr E.
1990
7 2 p. 257-263
7 p.
artikel
20 The α-A-crystallin and cystathionine β-synthase genes are physically very closely linked in proximal mouse chromosome 17 Stubbs, Lisa
1990
7 2 p. 284-288
5 p.
artikel
21 The human class I alcohol dehydrogenase gene cluster: Three genes are tandemly organized in an 80-kb-long segment of the genome Yasunami, Michio
1990
7 2 p. 152-158
7 p.
artikel
22 The Italian genome project Dulbecco, Renato
1990
7 2 p. 294-297
4 p.
artikel
23 Use of denaturing gradient gel electrophoresis for detection of mutation and prospective diagnosis in late onset ornithine transcarbamylase deficiency Finkelstein, Janice E.
1990
7 2 p. 167-172
6 p.
artikel
                             23 gevonden resultaten
 
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