| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A multilocus linkage map of mouse chromosome 8
|
Fletcher, Colin
|
|
1991
|
9 |
4 |
p. 737-741
5 p.
|
artikel
|
| 2 |
An improved pulsed-field polyacrylamide gel electrophoresis system for physical selection of linking clones: Isolation of SfiI linking clones from a chromosome 21-specific library
|
Ito, Takashi
|
|
1991
|
9 |
4 |
p. 707-712
6 p.
|
artikel
|
| 3 |
A proximal mouse chromosome 9 linkage map that further defines linkage groups homologous with segments of human chromosomes 11, 15, and 19
|
Seldin, Michael F.
|
|
1991
|
9 |
4 |
p. 678-685
8 p.
|
artikel
|
| 4 |
A serine-to-arginine (AGT-to-CGT) mutation in codon 549 of the CFTR gene in an Italian patient with severe cystic fibrosis
|
Sangiuolo, Federica
|
|
1991
|
9 |
4 |
p. 788-789
2 p.
|
artikel
|
| 5 |
Author index for volume 9
|
|
|
1991
|
9 |
4 |
p. 790-792
3 p.
|
artikel
|
| 6 |
cDNA and genomic cloning of HRC, a human sarcoplasmic reticulum protein, and localization of the gene to human chromosome 19 and mouse chromosome 7
|
Hofmann, Sandra L.
|
|
1991
|
9 |
4 |
p. 656-669
14 p.
|
artikel
|
| 7 |
Chromosomal assignment of one of the mammalian translation initiation factor eIF-4E genes
|
Dorfman, J.
|
|
1991
|
9 |
4 |
p. 785-788
4 p.
|
artikel
|
| 8 |
DNA Sequence, genomic organization, and chromosomal localization of the mouse peripheral myelin protein zero gene: Identification of polymorphic alleles
|
You, Kwan-Hee
|
|
1991
|
9 |
4 |
p. 751-757
7 p.
|
artikel
|
| 9 |
Gene mapping in marsupials: Detection of an ancient autosomal gene cluster
|
Sinclair, Andrew H.
|
|
1991
|
9 |
4 |
p. 581-586
6 p.
|
artikel
|
| 10 |
Genetic mapping of meander tail, a mouse mutation affecting cerebellar development
|
Fletcher, Colin
|
|
1991
|
9 |
4 |
p. 647-655
9 p.
|
artikel
|
| 11 |
Genetic mapping of the gene for a novel tyrosine kinase, Blk, to mouse chromosome 14
|
Kozak, Christine A.
|
|
1991
|
9 |
4 |
p. 762-764
3 p.
|
artikel
|
| 12 |
Genetic mapping of the Gs-α subunit gene (GNAS1) to the distal long arm of chromosome 20 using a polymorphism detected by denaturing gradient gel electrophoresis
|
Gejman, Pablo V.
|
|
1991
|
9 |
4 |
p. 782-783
2 p.
|
artikel
|
| 13 |
Genetic mapping of the mouse X chromosome in the region homologous to human Xq27–Xq28
|
Herman, Gail E.
|
|
1991
|
9 |
4 |
p. 670-677
8 p.
|
artikel
|
| 14 |
Hypervariable minisatellite DNA sequences in the Indian peafowl Pavo cristatus
|
Hanotte, Olivier
|
|
1991
|
9 |
4 |
p. 587-597
11 p.
|
artikel
|
| 15 |
In situ hybridization banding of human chromosomes with Alu-PCR products: A simultaneous karyotype for gene mapping studies
|
Baldini, Antonio
|
|
1991
|
9 |
4 |
p. 770-774
5 p.
|
artikel
|
| 16 |
Isolation and expression analysis of a human zinc finger gene (ZNF41) located on the short arm of the X chromosome
|
Franzè, Annamaria
|
|
1991
|
9 |
4 |
p. 728-736
9 p.
|
artikel
|
| 17 |
Linkage analysis in X-linked ocular albinism
|
Schnur, Rhonda E.
|
|
1991
|
9 |
4 |
p. 605-613
9 p.
|
artikel
|
| 18 |
Localization and genetic linkage of the human immunoglobulin heavy chain genes and the creatine kinase brain (CKB) gene: Identification of a hot spot for recombination
|
Benger, Judith C.
|
|
1991
|
9 |
4 |
p. 614-622
9 p.
|
artikel
|
| 19 |
Localization of Charcot-Marie-Tooth disease type 1a (CMT1A) to chromosome 17p11.2
|
Vance, Jeffery M.
|
|
1991
|
9 |
4 |
p. 623-628
6 p.
|
artikel
|
| 20 |
Localization of the zinc finger DNA-binding protein HIV-EP1/MBP-1/PRDII-BF1 to human chromosome 6p22.3–p24
|
Gaynor, Richard B.
|
|
1991
|
9 |
4 |
p. 758-761
4 p.
|
artikel
|
| 21 |
Localization of two genes encoding plasma membrane Ca2+-transporting ATPases to human chromosomes 1q25–32 and 12q21–23
|
Olson, Susan
|
|
1991
|
9 |
4 |
p. 629-641
13 p.
|
artikel
|
| 22 |
Mapping of facioscapulohumeral muscular dystrophy gene to chromosome 4q35-qter by multipoint linkage analysis and in situ hybridization
|
Wijmenga, Cisca
|
|
1991
|
9 |
4 |
p. 570-575
6 p.
|
artikel
|
| 23 |
Mapping of human chromosome 22 with a panel of somatic cell hybrids
|
Delattre, Olivier
|
|
1991
|
9 |
4 |
p. 721-727
7 p.
|
artikel
|
| 24 |
Mapping of the gene for X-linked liver glycogenosis due to phosphorylase kinase deficiency to human chromosome region Xp22
|
Willems, Patrick J.
|
|
1991
|
9 |
4 |
p. 565-569
5 p.
|
artikel
|
| 25 |
Molecular cloning and mapping of 10 new probes on the human Y chromosome
|
Nakahori, Y.
|
|
1991
|
9 |
4 |
p. 765-769
5 p.
|
artikel
|
| 26 |
Physical mapping of the genes for three components of the mouse DNA replication complex: Polymerase α to the X chromosome, primase p49 subunit to chromosome 10, and primase p58 subunit to chromosome 1
|
Adler, David A.
|
|
1991
|
9 |
4 |
p. 642-646
5 p.
|
artikel
|
| 27 |
Polymorphism due to variable number of repeats in the human involucrin gene
|
Simon, Marcia
|
|
1991
|
9 |
4 |
p. 576-580
5 p.
|
artikel
|
| 28 |
Rapid evolution of prostatic protein PSP94 suggested by sequence divergence between rhesus monkey and human cDNAs
|
Nolet, Serge
|
|
1991
|
9 |
4 |
p. 775-777
3 p.
|
artikel
|
| 29 |
Sixty-five radiation hybrids for the short arm of human chromosome 6: Their value as a mapping panel and as a source for rapid isolation of new probes using repeat element-mediated PCR
|
Zoghbi, Huda Y.
|
|
1991
|
9 |
4 |
p. 713-720
8 p.
|
artikel
|
| 30 |
The CEPH consortium linkage map of human chromosome 1
|
Dracopoli, Nicholas C.
|
|
1991
|
9 |
4 |
p. 686-700
15 p.
|
artikel
|
| 31 |
The human HPRT gene on a yeast artificial chromosome is functional when transferred to mouse cells by cell fusion
|
Huxley, Clare
|
|
1991
|
9 |
4 |
p. 742-750
9 p.
|
artikel
|
| 32 |
The mouse polycystic kidney disease mutation (cpk) is located on proximal chromosome 12
|
Davisson, Muriel T.
|
|
1991
|
9 |
4 |
p. 778-781
4 p.
|
artikel
|
| 33 |
The X chromosome of marsupials shares a highly conserved region with eutherians
|
Spencer, James A.
|
|
1991
|
9 |
4 |
p. 598-604
7 p.
|
artikel
|
| 34 |
Tight linkage between MPI and NP in baboons
|
van Oorschot, Roland A.H.
|
|
1991
|
9 |
4 |
p. 783-785
3 p.
|
artikel
|
| 35 |
Waisman syndrome, a human X-linked recessive basal ganglia disorder with mental retardation: Localization to Xq27.3-qter
|
Gregg, Ronald G.
|
|
1991
|
9 |
4 |
p. 701-706
6 p.
|
artikel
|
Tijdschrift beschrijving