13052_2019_718_MOESM1_ESM.doc (42 kB)

MOESM1 of NF1 microdeletion syndrome: case report of two new patients

journal contribution

posted on 2019-11-09, 05:11 authored by Gregorio Serra, Vincenzo Antona, Giovanni Corsello, Federico Zara, Ettore Piro, Raffaele Falsaperla

Additional file 1. Timelines of the clinical cases.

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NF1 gene Atypical deletion Genotype-phenotype correlation Contiguous gene syndrome MLPA

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