Concepedia

DNA diagnosis of Prader-Willi and Angelman syndromes with the probe PW71 (D15S63)

Ans M. W. van den Ouweland, Mieke N. van der Est, Eveline Wesby–van Swaay, Ton S. L. N. Tijmensen, Frans J. Los, J. O. Van Hemel, Raoul C. M. Hennekam, Hanne J. Meijers-Heijboer, Martinus F. Niermeijer, D. J. J. Halley

Human Genetics · 1995 · 18 citations · 24 references

DOI

Concepts

References

24

A simple salting out procedure for extracting DNA from human nucleated cells

S.A. Miller, Dale D. Dykes, Herbert F. Polesky · Nucleic Acids Research · 1988 · 20.6K citations · Full text

, , +8

DNA methylation represses <i>FMR-1</i> transcription in fragile X syndrome

James S. Sutcliffe, David L. Nelson, Fuping Zhang et al. · Human Molecular Genetics · 1992 · 681 citations

, , +15

Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader–Willi syndrome region

Stuart E. Leff, Camilynn I. Brannan, Martha L. Reed et al. · Nature Genetics · 1992 · 243 citations

, , +13

Imprinting mutations suggested by abnormal DNA methylation patterns in familial Angelman and Prader-Willi syndromes.

André Reis, Bärbel Dittrich, Valerie Greger et al. · PubMed · 1994 · 224 citations

, , +16

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