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Mouse Models of Genomic Syndromes as Tools for Understanding the Basis of Complex Traits: An Example with the Smith-Magenis and the Potocki-Lupski Syndromes

Each human's genome is distinguished by extra and missing DNA that can be “benign” or powerfully impact everything from development to disease. In the case of genomic disorders DNA rearrangements, such as deletions or duplications, correlate with a clinical specific phenotype. The clinical pres...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
मुख्य लेखकों: Carmona-Mora, P, Molina, J, Encina, C.A, Walz, K
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: Bentham Science Publishers Ltd. 2009
विषय:
ऑनलाइन पहुंच:https://ncbi.nlm.nih.gov/pmc/articles/PMC2709937/
https://ncbi.nlm.nih.gov/pubmed/19949547
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2174/138920209788488508
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