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source ID
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text
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# proj.
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# Ann.
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updated_at |
| PubMed |
10192393 |
A common human skin tumour is caused by activating mutations in beta-catenin.
WNT signalling orchest |
1.72 KB |
2015-10-29 |
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12 |
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14 |
2025-01-16
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| PubMed |
10190819 |
Mutational analysis and genotype-phenotype correlation of 29 unrelated Japanese patients with X-link |
2.59 KB |
2015-11-17 |
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9 |
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22 |
2025-01-16
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| PubMed |
144081 |
[Genetic heterogeneity of G6PD deficiency: mutant alleles of G6PD in the Shekii district of Azerbaij |
1022 Bytes |
2015-11-22 |
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9 |
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4 |
2025-01-16
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| PubMed |
6453040 |
[Gd- allele distribution patterns in Azerbaijan. III. The identification of mutant forms of glucose- |
759 Bytes |
2015-12-05 |
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8 |
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1 |
2025-01-16
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| PubMed |
10878391 |
Determination of carrier status for the Wiskott-Aldrich syndrome by flow cytometric analysis of Wisk |
1.27 KB |
2015-11-15 |
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10 |
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11 |
2025-01-16
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| PubMed |
2161209 |
Linkage of DNA markers at Xq28 to adrenoleukodystrophy and adrenomyeloneuropathy present within the |
985 Bytes |
2016-01-07 |
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10 |
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16 |
2025-01-16
|
| PubMed |
7959767 |
The murine homologues of the Huntington disease gene (Hdh) and the alpha-adducin gene (Add1) map to |
983 Bytes |
2015-11-27 |
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9 |
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4 |
2025-01-16
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| PubMed |
2562820 |
Linkage analysis of the apolipoprotein C2 gene and myotonic dystrophy on human chromosome 19 reveals |
1.49 KB |
2015-11-26 |
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12 |
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6 |
2025-01-16
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| PubMed |
10094552 |
A retrospective anonymous pilot study in screening newborns for HFE mutations in Scandinavian popula |
787 Bytes |
2015-11-02 |
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11 |
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1 |
2025-01-16
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| PubMed |
10484981 |
Hereditary TP53 codon 292 and somatic P16INK4A codon 94 mutations in a Li-Fraumeni syndrome family.
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1.73 KB |
2015-11-15 |
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17 |
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18 |
2025-01-16
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