Legius Syndrome - an overview
Por um escritor misterioso
Last updated 27 dezembro 2024
Genetic Clinics
Figure 2 from Legius syndrome, an Update. Molecular pathology of mutations in SPRED1.
Clinical features in 14 families with Legius syndrome
Café‐au‐lait macules and intertriginous freckling in piebaldism: Clinical overlap with neurofibromatosis type 1 and Legius syndrome - Stevens - 2012 - American Journal of Medical Genetics Part A - Wiley Online Library
Pediatric Dermatology Consult - December 2016
Legius Syndrome - an overview
Part 1: Café-au-lait macule – Presentation and genesis
Legius Syndrome - an overview
Legius syndrome
Table 1 from SPRED 1 Mutations in a Neurofibromatosis Clinic
DermNet - New page - Legius syndrome: a rare disorder characterised by café-au-lait macules. Read more
Noonan syndrome: improving recognition and diagnosis
Frontiers Novel pathogenic variants in KIT gene in three Chinese piebaldism patients
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