P59 Clinical diversity in 22q11.2 microdeletion syndrome & difficulties in diagnoses using only fluroscence in situ hybridisation (fish) | Archives of Disease in Childhood

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P59 Clinical diversity in 22q11.2 microdeletion syndrome & difficulties in diagnoses using only fluroscence in situ hybridisation (fish)

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Cite this article as:: Chauhan H, Plaiasu V, Diana O, et al

P59 Clinical diversity in 22q11.2 microdeletion syndrome & difficulties in diagnoses using only fluroscence in situ hybridisation (fish)

Archives of Disease in Childhood 2017;102:A56-A57.