Modeling Partial Monosomy for Human Chromosome 21q11.2-q21.1 Reveals Haploinsufficient Genes Influencing Behavior and Fat Deposition

Haploinsufficiency of part of human chromosome 21 results in a rare condition known as Monosomy 21. This disease displays a variety of clinical phenotypes, including intellectual disability, craniofacial dysmorphology, skeletal and cardiac abnormalities, and respiratory complications. To search for...

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Bibliografiska uppgifter
Huvudupphovsmän: Migdalska, Anna M., van der Weyden, Louise, Ismail, Ozama, White, Jacqueline K., Project, Sanger Mouse Genetics, Sánchez-Andrade, Gabriela, Logan, Darren W., Arends, Mark J., Adams, David J.
Materialtyp: Artigo
Språk:Inglês
Publicerad: Public Library of Science 2012
Ämnen:
Research Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC3262805/
https://ncbi.nlm.nih.gov/pubmed/22276124
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0029681
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