Journal of Medical Genetics 2009 (Volume 46 No 7) Contents Page

Fade Fave: SPRED1 germline mutations caused a neurofibromatosis type 1 overlapping phenotype

Fade Skinny: Identifies that National Institutes of Health diagnostic criteria for neurofibromatosis type 1 must be revised in view of newly characterised Legius syndrome in order to establish a specific genetic counselling.

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