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Crouzon syndrome with acanthosis nigricans and prominent diffuse hyperpigmentation associated with gain‐of‐function A391E mutation in FGFR3 gene. Issue 12 (29th August 2020)
Record Type:
Journal Article
Title:
Crouzon syndrome with acanthosis nigricans and prominent diffuse hyperpigmentation associated with gain‐of‐function A391E mutation in FGFR3 gene. Issue 12 (29th August 2020)
Main Title:
Crouzon syndrome with acanthosis nigricans and prominent diffuse hyperpigmentation associated with gain‐of‐function A391E mutation in FGFR3 gene