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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 |
16904497 |
Cauda equina syndrome after epidural steroid injection: a case report.
OBJECTIVE: Conventional treat |
1.65 KB |
2017-09-04 |
|
10 |
|
9 |
2021-12-23
|
| PubMed |
16970763 |
Mutations in the NDP gene: contribution to Norrie disease, familial exudative vitreoretinopathy and |
1.89 KB |
2015-11-20 |
|
11 |
|
9 |
2021-12-23
|
| PubMed |
17000021 |
No independent role of the -1123 G>C and+2740 A>G variants in the association of PTPN22 with type 1 |
2.11 KB |
2015-11-23 |
|
13 |
|
0 |
2021-12-23
|
| PubMed |
17033974 |
Mutation in the auxiliary calcium-channel subunit CACNA2D4 causes autosomal recessive cone dystrophy |
1.16 KB |
2015-11-23 |
|
18 |
|
5 |
2021-12-23
|
| PubMed |
1711760 |
Delayed institution of hypertension during focal cerebral ischemia: effect on brain edema.
The effec |
1.61 KB |
2015-12-23 |
|
9 |
|
6 |
2021-12-23
|
| PubMed |
17273972 |
Human TBX1 missense mutations cause gain of function resulting in the same phenotype as 22q11.2 dele |
1.11 KB |
2015-11-23 |
|
18 |
|
0 |
2021-12-23
|
| PubMed |
17286451 |
Retinoblastoma in India : microsatellite analysis and its application in genetic counseling.
OBJECTI |
1.73 KB |
2015-12-24 |
|
9 |
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0 |
2021-12-23
|
| PubMed |
17318851 |
Interferon regulatory factor 6 (IRF6) and fibroblast growth factor receptor 1 (FGFR1) contribute to |
1.5 KB |
2015-12-26 |
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10 |
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0 |
2021-12-23
|
| PubMed |
17327131 |
Molecular analysis of the CYP2F1 gene: identification of a frequent non-functional allelic variant.
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1.71 KB |
2015-12-28 |
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11 |
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1 |
2021-12-23
|
| PubMed |
17384765 |
Succimer chelation improves learning, attention, and arousal regulation in lead-exposed rats but pro |
1.79 KB |
2021-12-23 |
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8 |
|
10 |
2021-12-23
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