Highly restricted deletion of the SNORD116 region is implicated in Prader–Willi Syndrome - Concepedia

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Highly restricted deletion of the SNORD116 region is implicated in Prader–Willi Syndrome

DOI Full Paper Access

175

Citations

18

References

2014

Year

Éric Bieth, Sanaa Eddiry, Véronique Gaston, F. Lorenzini, Alexandre Buffet, Françoise Auriol, Catherine Molinas, Dorothée Cailley, Caroline Rooryck, Benoı̂t Arveiler,

European Journal of Human Genetics

Mendelian DisorderGenetic DisorderGeneticsPathogenesisPathologyMolecular GeneticsSnord116 RegionDisease Gene IdentificationPrader–willi SyndromeMedical GeneticsNeuropathologyMedicineNeurogenetics

References

	Year	Citations

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