Microdeletion of LIT1 in familial Beckwith-Wiedemann syndrome.

Niemitz EL, DeBaun MR, Fallon J, Murakami K, Kugoh H, Oshimura M, Feinberg AP
Am J Hum Genet. 2004 75 (5): 844-9

PMID: 15372379 · PMCID: PMC1182113 · DOI:10.1086/425343

MeSH Terms (14)

Beckwith-Wiedemann Syndrome Chromosomes, Human, Pair 11 Cyclin-Dependent Kinase Inhibitor p57 DNA Primers Gene Deletion Gene Expression Haplotypes Humans In Situ Hybridization, Fluorescence Karyotyping Membrane Proteins Nuclear Proteins Potassium Channels, Voltage-Gated Reverse Transcriptase Polymerase Chain Reaction

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