Concepedia

Clinical and Molecular Analysis of Five(Inv) Dup(15) Patients

Wendy P. Robinson, Franz Binkert, Ramon Giné, Carlos Vazquez, Wilfried Müller, W Rosenkranz, Albert Schinzel

European Journal of Human Genetics · 1993 · 174 citations · 20 references

DOI

Concepts

References

20

Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4.

D. Pinkel, J. E. Landegent, Colin C. Collins et al. · Proceedings of the National Academy of Sciences · 1988 · 1.3K citations · Full text

, , +17

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

Angelman and Prader‐Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion

Joan H.M. Knoll, Robert D. Nicholls, R.E. Magenis et al. · American Journal of Medical Genetics · 1989 · 583 citations

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Restriction sites containing CpG show a higher frequency of polymorphism in human DNA

David J.P. Barker, Markus Schäfer, R. White · Cell · 1984 · 582 citations

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Clinical and cytogenetic survey of 39 individuals with Prader‐Labhart‐Willi syndrome

Merlin G. Butler, F. John Meaney, Catherine G. Palmer et al. · American Journal of Medical Genetics · 1986 · 317 citations

, , +16