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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 |
15609295 |
Compound heterozygosity for a novel nine-nucleotide deletion and the Asn45Ser missense mutation in t |
1.39 KB |
2015-11-18 |
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34 |
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0 |
2021-12-23
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| PubMed |
15649253 |
Primary malignant lymphoma of the brain: frequent abnormalities and inactivation of p14 tumor suppre |
1.39 KB |
2015-11-18 |
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25 |
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0 |
2021-12-23
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| PubMed |
18674790 |
High fat diet-fed obese rats are highly sensitive to doxorubicin-induced cardiotoxicity.
Often, chem |
2.05 KB |
2021-11-28 |
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23 |
|
0 |
2021-12-23
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| 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 |
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0 |
2021-12-23
|
| PubMed |
16158428 |
Delineation of the clinical phenotype associated with OPHN1 mutations based on the clinical and neur |
898 Bytes |
2015-11-19 |
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25 |
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0 |
2021-12-23
|
| PubMed |
18166824 |
Genetic investigation of four meiotic genes in women with premature ovarian failure.
OBJECTIVE: The |
1.56 KB |
2015-11-23 |
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28 |
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0 |
2021-12-23
|
| PubMed |
16120104 |
A single-nucleotide polymorphism in the 5'-untranslated region of the hPER2 gene is associated with |
1.58 KB |
2015-11-19 |
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26 |
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0 |
2021-12-23
|
| PubMed |
16152606 |
Carrier frequency of mutation 657del5 in the NBS1 gene in a population of Polish pediatric patients |
1.76 KB |
2015-11-19 |
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29 |
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0 |
2021-12-23
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| PubMed |
16186368 |
Characterization of Bietti crystalline dystrophy patients with CYP4V2 mutations.
PURPOSE: Mutations |
1.8 KB |
2015-11-19 |
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26 |
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0 |
2021-12-23
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| PubMed |
15579441 |
Hypoxia in renal disease with proteinuria and/or glomerular hypertension.
Despite the increasing nee |
1.47 KB |
2015-11-22 |
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23 |
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0 |
2021-12-23
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