Concepedia

Minimum prevalence, birth incidence and cause of death for Prader–Willi syndrome in Flanders

Annick Vogels, Jenneke van den Ende, Kathelijn Keymolen, Geert Mortier, Koenraad Devriendt, Eric Legius, J P Fryns

European Journal of Human Genetics · 2003 · 185 citations · 11 references

DOI

Concepts

References

11

Genetic imprinting suggested by maternal heterodisomy in non-deletion Prader-Willi syndrome

Robert D. Nicholls, Joan H.M. Knoll, Merlin G. Butler et al. · Nature · 1989 · 887 citations

, , +11

Deletions of Chromosome 15 as a Cause of the Prader–Willi Syndrome

David H. Ledbetter, Vincent M. Riccardi, Susan Airhart et al. · New England Journal of Medicine · 1981 · 623 citations

, , +15

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

Molecular, cytogenetic, and clinical investigations of Prader-Willi syndrome patients

Wendy P. Robinson, Armand Bottani, J Balakrishman et al. · PubMed · 1991 · 280 citations · Full text

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Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 15q11-13

B�rbel Dittrich, WendyP. Robinson, Hans Knoblauch et al. · Human Genetics · 1992 · 203 citations

, , +13