Concepedia

Imprinting-Mutation Mechanisms in Prader-Willi Syndrome

Tohru Ohta, Todd A. Gray, Peter K. Rogan, Karin Buiting, James M. Gabriel, Shinji Saitoh, Bethi Muralidhar, B. Bilienska, Małgorzata Krajewska‐Walasek, Daniel J. Driscoll,

The American Journal of Human Genetics · 1999 · 276 citations · 43 references

DOIFull text

Open access

Concepts

References

43

Disruption of imprinting caused by deletion of the H19 gene region in mice

Philip A. Leighton, Robert S. Ingram, Jonathan Eggenschwiler et al. · Nature · 1995 · 759 citations

, , +9

Inherited microdeletions in the Angelman and Prader–Willi syndromes define an imprinting centre on human chromosome 15

Karin Buiting, Shinji Saitoh, Bärbel Dittrich et al. · Nature Genetics · 1995 · 598 citations

, , +16

Imprinted expression of the Igf2r gene depends on an intronic CpG island

Anton Wutz, Oskar W. Smrzka, Norbert Schweifer et al. · Nature · 1997 · 583 citations

, , +14

Epigenetic mechanisms underlying the imprinting of the mouse H19 gene.

Marisa S. Bartolomei, Andrea L. Webber, Mary E. Brunkow et al. · Genes & Development · 1993 · 488 citations · Full text

, , +15

Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region

James S. Sutcliffe, Mitsuyoshi Nakao, Susan L. Christian et al. · Nature Genetics · 1994 · 422 citations

, , +14