Suchergebnisse - "Colantoni, Luca"

PubPharm (2)

1

The variability of SMCHD1 gene in FSHD patients : evidence of new mutations

enthalten in: Human molecular genetics | 2019

von Strafella, C. | Caputo, V. | Galota, R. | +11

2

Facioscapulohumeral muscular dystrophy (FSHD) molecular diagnosis : from traditional technology to the NGS era

enthalten in: Neurogenetics | 2019

von Zampatti, S. | Colantoni, L. | Strafella, C. | +10

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