Microdeletion of LIT1 in Familial Beckwith-Wiedemann Syndrome

Beckwith-Wiedemann syndrome (BWS), which causes prenatal overgrowth, midline abdominal wall defects, macroglossia, and embryonal tumors, is a model for understanding the relationship between genomic imprinting, human development, and cancer. The causes are heterogeneous, involving multiple genes on...

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Huvudupphovsmän: Niemitz, Emily L., DeBaun, Michael R., Fallon, Jonathan, Murakami, Kazuhiro, Kugoh, Hiroyuki, Oshimura, Mitsuo, Feinberg, Andrew P.
Materialtyp: Artigo
Språk:Inglês
Publicerad: The American Society of Human Genetics 2004
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Articles
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC1182113/
https://ncbi.nlm.nih.gov/pubmed/15372379
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