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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 |
14510914 |
Congenital hypothyroidism due to a new deletion in the sodium/iodide symporter protein.
OBJECTIVE: I |
1.88 KB |
2015-11-18 |
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14 |
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4 |
2021-12-23
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| PubMed |
15041272 |
A first Taiwanese Chinese family of type 2B von Willebrand disease with R1306W mutation.
Clinical, l |
1.53 KB |
2015-11-18 |
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18 |
|
9 |
2021-12-23
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| PubMed |
15096016 |
Pallidal stimulation: an alternative to pallidotomy?
A resurgence of interest in the surgical treatm |
1.33 KB |
2021-12-23 |
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7 |
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2 |
2021-12-23
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| PubMed |
15099351 |
Mutations in the PCSK9 gene in Norwegian subjects with autosomal dominant hypercholesterolemia.
Prop |
1.09 KB |
2015-11-18 |
|
11 |
|
15 |
2021-12-23
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| PubMed |
15122708 |
Desmin-related myopathy with Mallory body-like inclusions is caused by mutations of the selenoprotei |
1.53 KB |
2015-11-18 |
|
10 |
|
11 |
2021-12-23
|
| PubMed |
15188772 |
Severe reversible left ventricular systolic and diastolic dysfunction due to accidental iatrogenic e |
830 Bytes |
2017-09-04 |
|
9 |
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0 |
2021-12-23
|
| PubMed |
15614572 |
Effects of the antidepressant trazodone, a 5-HT 2A/2C receptor antagonist, on dopamine-dependent beh |
1.92 KB |
2015-11-22 |
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7 |
|
7 |
2021-12-23
|
| PubMed |
15623763 |
TGFBI gene mutations causing lattice and granular corneal dystrophies in Indian patients.
PURPOSE: T |
1.89 KB |
2015-11-18 |
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12 |
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11 |
2021-12-23
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| PubMed |
15818664 |
Association of sporadic chondrocalcinosis with a -4-basepair G-to-A transition in the 5'-untranslate |
2.28 KB |
2015-11-19 |
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10 |
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20 |
2021-12-23
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| PubMed |
15824163 |
No Evidence for BRAF as a melanoma/nevus susceptibility gene.
Somatic mutations of BRAF have been id |
1.75 KB |
2015-11-19 |
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11 |
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15 |
2021-12-23
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