| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A graphical representation of genetic and physical maps: The Marey map
|
Chakravarti, Aravinda
|
|
1991
|
11 |
1 |
p. 219-222
4 p.
|
artikel
|
| 2 |
A 2.5-Mb physical map within 3p21.1 spans the breakpoint associated with greig cephalopolysyndactyly syndrome
|
Gemmill, Robert M.
|
|
1991
|
11 |
1 |
p. 93-102
10 p.
|
artikel
|
| 3 |
A population genetic study of six VNTR loci in three ethnically defined populations
|
Deka, Ranjan
|
|
1991
|
11 |
1 |
p. 83-92
10 p.
|
artikel
|
| 4 |
Assignment of the human prohibition gene (PHB) to chromosome 17 and identification of a DNA polymorphism
|
White, John J.
|
|
1991
|
11 |
1 |
p. 228-230
3 p.
|
artikel
|
| 5 |
Assignment of the YT blood group locus to chromosome 7q
|
Zelinski, T.
|
|
1991
|
11 |
1 |
p. 165-167
3 p.
|
artikel
|
| 6 |
Autosomal dominant retinitis pigmentosa: Four new mutations in rhodopsin, one of them in the retinal attachment site
|
Keen, T.J.
|
|
1991
|
11 |
1 |
p. 199-205
7 p.
|
artikel
|
| 7 |
Characterization of a set of variable number of tandem repeat markers conserved in Bovidae
|
Georges, Michel
|
|
1991
|
11 |
1 |
p. 24-32
9 p.
|
artikel
|
| 8 |
Chromosomal assignments of the genes for neuroendocrine convertase PC1 (NEC1) to human 5q15–21, neuroendocrine convertase PC2 (NEC2) to human 20p11.1–11.2, and furin (mouse 7[D1-E2] region)
|
Seidah, Nabil G.
|
|
1991
|
11 |
1 |
p. 103-107
5 p.
|
artikel
|
| 9 |
Chromosomal deletion 4p15.32→p14 in a treacher collins syndrome patient: Exclusion of the disease locus from and mapping of anonymous DNA sequences to this region
|
Jabs, Ethylin Wang
|
|
1991
|
11 |
1 |
p. 188-192
5 p.
|
artikel
|
| 10 |
Chromosomal mapping of A1 and A2 adenosine receptors, VIP receptor, and a new subtype of serotonin receptor
|
Libert, Frédérick
|
|
1991
|
11 |
1 |
p. 225-227
3 p.
|
artikel
|
| 11 |
Chromosome-specific alpha satellites: Two distinct families on human chromosome 18
|
Alexandrov, I.A.
|
|
1991
|
11 |
1 |
p. 15-23
9 p.
|
artikel
|
| 12 |
Cloning and sequence analysis of a human Y-chromosome-derived, testicular cDNA, TSPY
|
Arnemann, Joachim
|
|
1991
|
11 |
1 |
p. 108-114
7 p.
|
artikel
|
| 13 |
Construction and characterization of a Notl-BsuE linking library from the human X chromosome
|
Arenstorf, Hartwig P.
|
|
1991
|
11 |
1 |
p. 115-123
9 p.
|
artikel
|
| 14 |
Direct sequencing of the dopamine D2 receptor (DRD2) in schizophrenics reveals three polymorphisms but no structural change in the receptor
|
Sarkar, Gobinda
|
|
1991
|
11 |
1 |
p. 8-14
7 p.
|
artikel
|
| 15 |
Human clathrin heavy chain (CLTC): Partial molecular cloning, expression, and mapping of the gene to human chromosome 17q11-qter
|
Dodge, George R.
|
|
1991
|
11 |
1 |
p. 174-178
5 p.
|
artikel
|
| 16 |
Human glandular kallikrein genes: Genetic and physical mapping of the KLK1 locus using a highly polymorphic microsatellite PCR marker
|
Richards, Robert I.
|
|
1991
|
11 |
1 |
p. 77-82
6 p.
|
artikel
|
| 17 |
In vitro mutagenesis helps to unravel the biological consequences of aspartylglucosaminuria mutation
|
Ikonen, Elina
|
|
1991
|
11 |
1 |
p. 206-211
6 p.
|
artikel
|
| 18 |
Isolation of a human chromosome 14-only somatic cell hybrid: Analysis using Alu and LINE-based PCR
|
Mares Jr., Adolph
|
|
1991
|
11 |
1 |
p. 215-218
4 p.
|
artikel
|
| 19 |
Localization of 616 human chromosome 3-specific cosmids using a somatic cell hybrid deletion mapping panel
|
Smith, David I.
|
|
1991
|
11 |
1 |
p. 179-187
9 p.
|
artikel
|
| 20 |
Mapping the Treacher Collins syndrome locus to 5q31.3→q33.3
|
Wang Jabs, Ethylin
|
|
1991
|
11 |
1 |
p. 193-198
6 p.
|
artikel
|
| 21 |
Molecular analysis of overlapping chromosomal deletions in patients with Langer-Giedion syndrome
|
Parrish, Julia E.
|
|
1991
|
11 |
1 |
p. 54-61
8 p.
|
artikel
|
| 22 |
Molecular genetic linkage maps of mouse chromosomes 4 and 6
|
Bahary, Nathan
|
|
1991
|
11 |
1 |
p. 33-47
15 p.
|
artikel
|
| 23 |
Nucleotide sequence of the 3′ nuclease-sensitive region of the human phosphoglycerate kinase 1 (PGK1) gene
|
Riley, Donald E.
|
|
1991
|
11 |
1 |
p. 212-214
3 p.
|
artikel
|
| 24 |
Patterns of DNA methylation are indistinguishable in different individuals over a wide range of human DNA sequences
|
Behn-Krappa, Annett
|
|
1991
|
11 |
1 |
p. 1-7
7 p.
|
artikel
|
| 25 |
Physical mapping of the loci Gabra3, DXPas8, CamL1, and Rsvp in a region of the mouse X chromosome homologous to human Xq28
|
Faust, Cynthia J.
|
|
1991
|
11 |
1 |
p. 154-164
11 p.
|
artikel
|
| 26 |
Seven novel Tay-Sachs mutations detected by chemical mismatch cleavage of PCR-amplified cDNA fragments
|
Akli, Saïd
|
|
1991
|
11 |
1 |
p. 124-134
11 p.
|
artikel
|
| 27 |
Simultaneous screening for β-thalassemia mutations by chemical cleavage of mismatch
|
Dianzani, Irma
|
|
1991
|
11 |
1 |
p. 48-53
6 p.
|
artikel
|
| 28 |
The exon organization of the triple-helical coding regions of the human α1(VI) and α2(VI) collagen genes is highly similar
|
Saitta, Biagio
|
|
1991
|
11 |
1 |
p. 145-153
9 p.
|
artikel
|
| 29 |
The 5-HT2 serotonin receptor gene Htr-2 is tightly linked to Es-10 on mouse chromosome 14
|
Liu, Jian
|
|
1991
|
11 |
1 |
p. 231-234
4 p.
|
artikel
|
| 30 |
The human homolog of the mouse common viral integration region, FLI1, maps to 11q23–q24
|
Baud, Véronique
|
|
1991
|
11 |
1 |
p. 223-224
2 p.
|
artikel
|
| 31 |
The Sp1 transcription factor gene (SP1) and the 1,25-dihydroxyvitamin D3 receptor gene (VDR) are colocalized on human chromosome arm 12q and rat chromosome 7
|
Szpirer, Josiane
|
|
1991
|
11 |
1 |
p. 168-173
6 p.
|
artikel
|
| 32 |
The structure of the mouse lipoprotein lipase gene: A B1 repetitive element is inserted into the 3′ untranslated region of the mRNA
|
Zechner, R.
|
|
1991
|
11 |
1 |
p. 62-76
15 p.
|
artikel
|
| 33 |
The use of synthetic tandem repeats to isolate new VNTR loci: Cloning of a human hypermutable sequence
|
Vergnaud, Gilles
|
|
1991
|
11 |
1 |
p. 135-144
10 p.
|
artikel
|
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