Fryns syndrome phenotype caused by chromosome microdeletions at 15q26.2 and 8p23.1 | Journal of Medical Genetics

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Fryns syndrome phenotype caused by chromosome microdeletions at 15q26.2 and 8p23.1

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Cite this article as:: Slavotinek A, Lee SS, Davis R, et al

Fryns syndrome phenotype caused by chromosome microdeletions at 15q26.2 and 8p23.1

Journal of Medical Genetics 2005;42:730-736.