Epimutations in Prader-Willi and Angelman Syndromes: A Molecular Study of 136 Patients with an Imprinting Defect - Concepedia

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Publication | Open Access

Epimutations in Prader-Willi and Angelman Syndromes: A Molecular Study of 136 Patients with an Imprinting Defect

DOI Full Paper Access

366

Citations

20

References

2003

Year

Karin Buiting, Stephanie Groß, Christina Lich, Gabriele Gillessen‐Kaesbach, Osman El‐Maarri, Bernhard Horsthemke

The American Journal of Human Genetics

Imprinting DefectMolecular StudyAngelman Syndromes

References

	Year	Citations

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