Concepedia

Balanced Translocation 46, XY, t(2;15)(q37.2;q11.2) Associated with Atypical Prader-Willi Syndrome

Jeffrey M. Conroy, Theresa A. Grebe, Laurie A. Becker, Karen D. Tsuchiya, Robert D. Nicholls, Karin Buiting, Bernhard Horsthemke, Suzanne B. Cassidy, Stuart Schwartz

The American Journal of Human Genetics · 1997 · 58 citations · 25 references

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25

Prader-Willi Syndrome: Consensus Diagnostic Criteria

Vanja A. Holm, Suzanne B. Cassidy, Merlin G. Butler et al. · PEDIATRICS · 1993 · 1.3K citations · Full text

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A routine method for the establishment of permanent growing lymphoblastoid cell lines

Heidemarie Neitzel · Human Genetics · 1986 · 647 citations

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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

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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

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Prader‐Willi syndrome: Current understanding of cause and diagnosis

Merlin G. Butler · American Journal of Medical Genetics · 1990 · 579 citations · Full text

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