DOI: 10.1055/s-00029027

Journal of Pediatric Genetics

References

Nemes E, Farkas K, Kocsis-Deák B. , et al.
Phenotypical diversity of patients with LEOPARD syndrome carrying the worldwide recurrent p.Tyr279Cys PTPN11 mutation.

Arch Dermatol Res 2015;
307 (10) 891-895

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