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                             40 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A genetic linkage map of 32 loci on human chromosome 10 Bowden, Donald W.
1989
5 4 p. 718-726
9 p.
artikel
2 A genetic linkage map of markers for human chromosome 20 Nakamura, Yusuke
1989
5 4 p. 945-947
3 p.
artikel
3 A highly polymorphic locus cloned from the breakpoint of a chromosome 11p13 deletion associated with the WAGR syndrome Glaser, Tom
1989
5 4 p. 880-893
14 p.
artikel
4 A human alphoid DNA clone from the EcoRI dimeric family: Genomic and internal organization and chromosomal assignment Baldini, A.
1989
5 4 p. 822-828
7 p.
artikel
5 A molecular genetic linkage map of mouse chromosome 4 including the localization of several proto-oncogenes Ceci, Jeffrey D.
1989
5 4 p. 699-709
11 p.
artikel
6 An analysis of variation in the long-range genomic organization of the human major histocompatibility complex class II region by pulsed-field gel electrophoresis Dunham, Ian
1989
5 4 p. 787-796
10 p.
artikel
7 A new DNA marker (D4S90) is located terminally on the short arm of chromosome 4, close to the Huntington disease gene Youngman, Sandra
1989
5 4 p. 802-809
8 p.
artikel
8 Assignment of the αB-crystallin gene to human chromosome 11 Ngo, Julielani T.
1989
5 4 p. 665-669
5 p.
artikel
9 Assignment of the gene for complete X-linked congenital stationary night blindness (CSNB1) to Xp11.3 Musarella, M.A.
1989
5 4 p. 727-737
11 p.
artikel
10 Author index for volume 5 1989
5 4 p. 958-960
3 p.
artikel
11 Characterization of a highly unstable mouse minisatellite locus: Evidence for somatic mutation during early development Kelly, Robert
1989
5 4 p. 844-856
13 p.
artikel
12 Characterization of eight VNTR loci by agarose gel electrophoresis Odelberg, S.J.
1989
5 4 p. 915-924
10 p.
artikel
13 Chromosome mapping of the human ras-related rab3A gene to 19p13.2 Rousseau-Merck, M.F.
1989
5 4 p. 694-698
5 p.
artikel
14 Complementation of repair gene mutations on the hemizygous chromosome 9 in CHO: A third repair gene on human chromosome 19 Thompson, Larry H.
1989
5 4 p. 670-679
10 p.
artikel
15 Complete human rDNA repeat units isolated in yeast artificial chromosomes Labella, Tullio
1989
5 4 p. 752-760
9 p.
artikel
16 CpG dinucleotides are mutation hot spots in phenylketonuria Abadie, Véronique
1989
5 4 p. 936-939
4 p.
artikel
17 CpG islands surround a DNA segment located between translocation breakpoints associated with genitourinary dysplasia and aniridia Bickmore, Wendy A.
1989
5 4 p. 685-693
9 p.
artikel
18 Cumulative subject index volumes 4–5 1989
5 4 p. 961-977
17 p.
artikel
19 Definition of mouse chromosome 1 and 3 gene linkage groups that are conserved on human chromosome 1: Evidence that a conserved linkage group spans the centromere of human chromosome 1 Moseley, Walton S.
1989
5 4 p. 899-905
7 p.
artikel
20 Deletion mapping of DNA markers to a region of chromosome 5 that cosegregates with schizophrenia Gilliam, T.Conrad
1989
5 4 p. 940-944
5 p.
artikel
21 Errata 1989
5 4 p. 957-
1 p.
artikel
22 Genomic structure of the human cytosolic aldehyde dehydrogenase gene Hsu, Lily C.
1989
5 4 p. 857-865
9 p.
artikel
23 Haplotypes in cystic fibrosis patients with or without pancreatic insufficiency from four European populations Devoto, M.
1989
5 4 p. 894-898
5 p.
artikel
24 Howard hughes medical institute and its role in genomic activities Cahill Jr., George F.
1989
5 4 p. 952-954
3 p.
artikel
25 Human laminin a chain (LAMA) gene: Chromosomal mapping to locus 18p11.3 Nagayoshi, Toshiro
1989
5 4 p. 932-935
4 p.
artikel
26 Human-mouse hybrids carrying fragments of single human chromosomes selected by tumor growth Porteous, David J.
1989
5 4 p. 680-684
5 p.
artikel
27 Linkage map of mouse chromosome 17: Localization of 27 new DNA markers Vincek, Vladimir
1989
5 4 p. 773-786
14 p.
artikel
28 Patterns of intra- and interarray sequence variation in alpha satellite from the human X chromosome: Evidence for short-range homogenization of tandemly repeated DNA sequences Durfy, Sharon J.
1989
5 4 p. 810-821
12 p.
artikel
29 Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction Orita, Masato
1989
5 4 p. 874-879
6 p.
artikel
30 Recombination events that locate myotonic dystrophy distal to APOC2 on 19q Johnson, Keith
1989
5 4 p. 746-751
6 p.
artikel
31 Simultaneous genetic mapping of multiple human minisatellite sequences using DNA fingerprinting Wells, Richard A.
1989
5 4 p. 761-772
12 p.
artikel
32 Structure and expression of the rat class I alcohol dehydrogenase gene Crabb, David W.
1989
5 4 p. 906-914
9 p.
artikel
33 The gene for human muscle-specific phosphoglycerate mutase, PGAM2, mapped to chromosome 7 by polymerase chain reaction Edwards, Yvonne H.
1989
5 4 p. 948-951
4 p.
artikel
34 The human ATP synthase β subunit gene: Sequence analysis, chromosome assignment, and differential expression Neckelmann, Nicolas
1989
5 4 p. 829-843
15 p.
artikel
35 The human α2(XI) collagen gene (COL11A2) maps to the centromeric border of the major histocompatibility complex on chromosome 6 Hanson, Isabel M.
1989
5 4 p. 925-931
7 p.
artikel
36 The polymorphic marker DXS304 is within 5 centimorgans of the fragile X locus Vincent, A.
1989
5 4 p. 797-801
5 p.
artikel
37 The proximity of DNA sequences in interphase cell nuclei is correlated to genomic distance and permits ordering of cosmids spanning 250 kilobase pairs Trask, Barbara
1989
5 4 p. 710-717
8 p.
artikel
38 The Santa Cruz Workshop—May 1985 Sinsheimer, Robert L.
1989
5 4 p. 954-956
3 p.
artikel
39 Twenty-five loci form a continuous linkage map of markers for human chromosome 7 Lathrop, G.Mark
1989
5 4 p. 866-873
8 p.
artikel
40 Twenty loci form a continuous linkage map of markers for human chromosome 2 O'Connell, P.
1989
5 4 p. 738-745
8 p.
artikel
                             40 gevonden resultaten
 
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