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Association of copy number variation in the FCGR3B gene with risk of autoimmune diseases
Copy number variation (CNV) of human DNA segments is an important source of genetic diversity and increasing evidence indicates that CNV may underlie disease susceptibility.1–4 It is to be noted that there seems to be an ...
Genomic Imbalances In Syndromic Congenital Heart Disease
(Elsevier Editora Ltda, 2016)
Mitochondrial DNA deletions detected by Multiplex Ligation-dependent Probe Amplification
(Informa Healthcare, 2015-06)
The genetic diagnosis algorithm for mitochondrial (mt) diseases starts looking for deletions and common mutations in mtDNA. MtDNA's special features, such as large and variable genome copies, heteroplasmy, polymorphisms, ...
Initial analysis of copy number variations in canchim beef cattle with extreme phenotypes for ribeye area.
(In: INTERNATIONAL PLANT & ANIMAL GENOME, 21., 2013, San Diego. [Abstracts]... [S.l.: s.n.], 2013., 2013)
Initial analysis of copy number variations in canchim beef cattle with extreme phenotypes for ribeye area.
(In: INTERNATIONAL PLANT & ANIMAL GENOME, 21., 2013, San Diego. [Abstracts]... [S.l.: s.n.], 2013., 2013)
Genomic copy number variation associated with clinical outcome in canine cutaneous mast cell tumors
(2017-04-01)
Mast cell tumors are the most common malignant cutaneous tumors in dogs. Although there are several prognostic factors involved, the clinical and biological behavior of this type of tumor varies greatly, making the best ...