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source DB |
source ID
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text
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size
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updated at |
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# proj.
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# Ann.
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updated_at |
| PubMed |
20651814 |
Lack of association between ADRA2B-4825 gene insertion/deletion polymorphism and migraine in Chinese |
1.02 KB |
2015-11-25 |
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27 |
|
6 |
2021-12-22
|
| PubMed |
20534762 |
Two novel mutations of the TSH-beta subunit gene underlying congenital central hypothyroidism undete |
1.82 KB |
2016-01-02 |
|
33 |
|
7 |
2021-12-22
|
| PubMed |
20523265 |
Association study of complement factor H, C2, CFB, and C3 and age-related macular degeneration in a |
2.3 KB |
2015-11-25 |
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29 |
|
13 |
2021-12-22
|
| PubMed |
20126413 |
U87MG decoded: the genomic sequence of a cytogenetically aberrant human cancer cell line.
U87MG is a |
2.07 KB |
2016-01-01 |
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26 |
|
6 |
2021-12-22
|
| PubMed |
20005218 |
A potential regulatory single nucleotide polymorphism in the promoter of the Klotho gene may be asso |
1.67 KB |
2015-11-25 |
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28 |
|
13 |
2021-12-22
|
| PubMed |
19394258 |
The first founder DGUOK mutation associated with hepatocerebral mitochondrial DNA depletion syndrome |
1.57 KB |
2015-11-25 |
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29 |
|
5 |
2021-12-22
|
| PubMed |
19365571 |
Macular corneal dystrophy in a Chinese family related with novel mutations of CHST6.
PURPOSE: To ide |
1.85 KB |
2015-11-25 |
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29 |
|
3 |
2021-12-22
|
| PubMed |
19101703 |
Study of a Taiwanese family with oculopharyngeal muscular dystrophy.
BACKGROUND: Oculopharyngeal mus |
1.2 KB |
2015-11-24 |
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26 |
|
11 |
2021-12-22
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| PubMed |
19082493 |
Combination of polymorphisms within 5' and 3' untranslated regions of thymidylate synthase gene modu |
2.15 KB |
2015-08-06 |
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25 |
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11 |
2021-12-22
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| PubMed |
19037252 |
Mutations in phospholipase C epsilon 1 are not sufficient to cause diffuse mesangial sclerosis.
Diff |
1.06 KB |
2015-11-24 |
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29 |
|
8 |
2021-12-22
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