| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A long-range restriction map of the interleukin-4 and interleukin-5 linkage group on chromosome 5
|
Chandrasekharappa, Settara C.
|
|
1990
|
6 |
1 |
p. 94-99
6 p.
|
artikel
|
| 2 |
A method of sequencing without subcloning and its application to the identification of a novel ORF with a sequence suggestive of a transcriptional regulator in the water mold Achlya ambisexualis
|
Schowalter, David B.
|
|
1990
|
6 |
1 |
p. 23-32
10 p.
|
artikel
|
| 3 |
Amplification of a long sequence that includes a processed pseudogene for elongation factor 2 in the mouse
|
Koide, Tsuyoshi
|
|
1990
|
6 |
1 |
p. 80-88
9 p.
|
artikel
|
| 4 |
A new polymorphic locus, D7S411, isolated by cloning from preparative pulse-field gels is close to the mutation causing cystic fibrosis
|
Ramsay, M.
|
|
1990
|
6 |
1 |
p. 39-47
9 p.
|
artikel
|
| 5 |
An interspecific backcross linkage map of mouse chromosome 8
|
Ceci, Jeffrey D.
|
|
1990
|
6 |
1 |
p. 72-79
8 p.
|
artikel
|
| 6 |
A panel of irradiation-reduced hybrids selectively retaining human chromosome 11p13: Their structure and use to purify the WAGR gene complex
|
Glaser, Tom
|
|
1990
|
6 |
1 |
p. 48-64
17 p.
|
artikel
|
| 7 |
Characterization of mutations in the factor VIII gene by direct sequencing of amplified genomic DNA
|
Higuchi, Miyoko
|
|
1990
|
6 |
1 |
p. 65-71
7 p.
|
artikel
|
| 8 |
Chromosomal organization and localization of the human urokinase inhibitor gene: Perfect structural conservation with ovalbumin
|
Samia, Julie A.
|
|
1990
|
6 |
1 |
p. 159-167
9 p.
|
artikel
|
| 9 |
Complete cDNA sequence and chromosomal localization of mouse α 1-antitrypsin
|
Sifers, Richard N.
|
|
1990
|
6 |
1 |
p. 100-104
5 p.
|
artikel
|
| 10 |
Direct sequencing of the activation peptide and the catalytic domain of the factor IX gene in six species
|
Sarkar, G.
|
|
1990
|
6 |
1 |
p. 133-143
11 p.
|
artikel
|
| 11 |
Genomic mapping of murine Zp-2 and Zp-3, two oocyte-specific loci encoding zona pellucida proteins
|
Dwayne Lunsford, R.
|
|
1990
|
6 |
1 |
p. 184-187
4 p.
|
artikel
|
| 12 |
Human arylsulfatase B: MOPAC cloning, nucleotide sequence of a full-length cDNA, and regions of amino acid identity with arylsulfatases A and C
|
Schuchman, Edward H.
|
|
1990
|
6 |
1 |
p. 149-158
10 p.
|
artikel
|
| 13 |
Mapping of a gene determining tuberous sclerosis to human chromosome 11q1411q23
|
Smith, Moyra
|
|
1990
|
6 |
1 |
p. 105-114
10 p.
|
artikel
|
| 14 |
New polymorphic DNA marker close to the fragile site FRAXA
|
Oostra, B.A.
|
|
1990
|
6 |
1 |
p. 129-132
4 p.
|
artikel
|
| 15 |
no evidence for linkage between late onset autosomal dominant retinitis pigmentosa and chromosome 3 locus D3S47 (C17): Evidence for genetic heterogeneity
|
Inglehearn, C.F.
|
|
1990
|
6 |
1 |
p. 168-173
6 p.
|
artikel
|
| 16 |
Ornithine aminotransferase (OAT): Recombination between an X-linked OAT sequence (7.5 kb) and the Norrie disease locus
|
Ngo, Julielani T.
|
|
1990
|
6 |
1 |
p. 123-128
6 p.
|
artikel
|
| 17 |
Physical mapping of probes within 14q32, a subtelomeric region showing a high recombination frequency
|
Hofker, Marten H.
|
|
1990
|
6 |
1 |
p. 33-38
6 p.
|
artikel
|
| 18 |
Physical maps of 4p16.3, the area expected to contain the Huntington disease mutation
|
Bućan, M.
|
|
1990
|
6 |
1 |
p. 1-15
15 p.
|
artikel
|
| 19 |
Rare HRAS alleles and susceptibility to human breast cancer
|
Hall, Jeffrey M.
|
|
1990
|
6 |
1 |
p. 188-191
4 p.
|
artikel
|
| 20 |
Repetitive DNA (TGGA) n 5′ to the human myelin basic protein gene: A new form of oligonucleotide repetitive sequence showing length polymorphism
|
Boylan, Kevin B.
|
|
1990
|
6 |
1 |
p. 16-22
7 p.
|
artikel
|
| 21 |
Sequences homologous to glutamic acid decarboxylase cDNA are present on mouse chromosomes 2 and 10
|
Brilliant, Murray H.
|
|
1990
|
6 |
1 |
p. 115-122
8 p.
|
artikel
|
| 22 |
Somatic cell genetic analysis of human cell surface antigens 5.1H11 and F35 9 (gp45)
|
Rettig, Wolfgang J.
|
|
1990
|
6 |
1 |
p. 178-183
6 p.
|
artikel
|
| 23 |
The gene for the muscle-specific enolase is on the short arm of human chromosome 17
|
Feo, Salvatore
|
|
1990
|
6 |
1 |
p. 192-194
3 p.
|
artikel
|
| 24 |
The human metallothionein gene cluster is not disrupted in myelomonocytic leukemia
|
Sutherland, Grant R.
|
|
1990
|
6 |
1 |
p. 144-148
5 p.
|
artikel
|
| 25 |
The locus for Japanese myotonic dystrophy is also linked to D19S19 on the long arm of chromosome 19
|
Takemoto, Juji
|
|
1990
|
6 |
1 |
p. 195-196
2 p.
|
artikel
|
| 26 |
The locus for the medium-chain acyl-CoA dehydrogenase gene on chromosome 1 is highly polymorphic
|
Kidd, Judith R.
|
|
1990
|
6 |
1 |
p. 89-93
5 p.
|
artikel
|
| 27 |
The neuroepithelioma breakpoint on chromosome 22 is proximal to the meningioma locus
|
Zhang, F.R.
|
|
1990
|
6 |
1 |
p. 174-177
4 p.
|
artikel
|
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