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source DB |
source ID
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text
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updated at |
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# proj.
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# Ann.
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updated_at |
| PubMed |
19477219 |
Identified hidden genomic changes in mantle cell lymphoma using high-resolution single nucleotide po |
1.85 KB |
2015-11-25 |
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5 |
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0 |
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| PubMed |
19110214 |
A recessive skeletal dysplasia, SEMD aggrecan type, results from a missense mutation affecting the C |
1.78 KB |
2015-11-24 |
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6 |
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2 |
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| PubMed |
18827003 |
A novel point mutation in the amino terminal domain of the human glucocorticoid receptor (hGR) gene |
1.77 KB |
2015-08-06 |
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2 |
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6 |
-
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| PubMed |
18398821 |
Genome-wide analysis identifies 16q deletion associated with survival, molecular subtypes, mRNA expr |
1.41 KB |
2015-08-06 |
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1 |
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0 |
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| PubMed |
18266724 |
Histamine-N-methyl transferase polymorphism and risk for migraine.
BACKGROUND/OBJECTIVES: Histamine |
1.14 KB |
2015-11-24 |
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3 |
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2 |
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| PubMed |
17437275 |
Novel mutations in the ZEB1 gene identified in Czech and British patients with posterior polymorphou |
1.13 KB |
2015-11-23 |
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5 |
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0 |
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| PubMed |
17003923 |
Gene polymorphisms implicated in influencing susceptibility to venous and arterial thromboembolism: |
2.03 KB |
2015-11-23 |
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5 |
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12 |
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| PubMed |
16840830 |
Two novel mutations in the MEN1 gene in subjects with multiple endocrine neoplasia-1.
Multiple endoc |
1.34 KB |
2015-11-23 |
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26 |
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2 |
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| PubMed |
16288197 |
Genetic homogeneity for inherited congenital microcoria loci in an Asian Indian pedigree.
PURPOSE: C |
2.59 KB |
2015-11-19 |
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29 |
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4 |
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| PubMed |
15353880 |
Fabry disease female proband with clinical manifestations similar to hypertrophic cardiomyopathy.
Fa |
1 KB |
2015-11-22 |
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8 |
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0 |
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