Clinical phenotypes of MAGEL2 mutations and deletions

Karin Buiting; Nataliya Di Donato; Jasmin Beygo; Susanne Bens; Maja Von Der Hagen; Karl Hackmann; Bernhard Horsthemke

ArticleOPEN ACCESS

Clinical phenotypes of MAGEL2 mutations and deletions

Buiting K
Di Donato N
Beygo J
et al.

Orphanet Journal of Rare Diseases

DOI: 10.1186/1750-1172-9-40

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APA

Buiting, K., Di Donato, N., Beygo, J., Bens, S., Von Der Hagen, M., Hackmann, K., & Horsthemke, B. (2014, March 25). Clinical phenotypes of MAGEL2 mutations and deletions. Orphanet Journal of Rare Diseases. BioMed Central Ltd. https://doi.org/10.1186/1750-1172-9-40

Clinical phenotypes of MAGEL2 mutations and deletions

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