Generation and Comparative Analysis of ∼3.3 Mb of Mouse Genomic Sequence Orthologous to the Region of Human Chromosome 7q11.23 Implicated in Williams Syndrome

Williams syndrome is a complex developmental disorder that results from the heterozygous deletion of a ∼1.6-Mb segment of human chromosome 7q11.23. These deletions are mediated by large (∼300 kb) duplicated blocks of DNA of near-identical sequence. Previously, we showed that the orthologous region o...

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Detalhes bibliográficos
Main Authors: DeSilva, Udaya, Elnitski, Laura, Idol, Jacquelyn R., Doyle, Johannah L., Gan, Weiniu, Thomas, James W., Schwartz, Scott, Dietrich, Nicole L., Beckstrom-Sternberg, Stephen M., McDowell, Jennifer C., Blakesley, Robert W., Bouffard, Gerard G., Thomas, Pamela J., Touchman, Jeffrey W., Miller, Webb, Green, Eric D.
Formato: Artigo
Idioma:Inglês
Publicado em: Cold Spring Harbor Laboratory Press 2002
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Reports
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC155257/
https://ncbi.nlm.nih.gov/pubmed/11779826
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/gr.214802
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