Legius Syndrome - an overview
Por um escritor misterioso
Last updated 10 junho 2024
Café-Au-Lait Macules and Macrocephaly in a 19-Month-Old: Diagnostic Considerations Beyond Neurofibromatosis – Consult QD
News The RASopathies Network
AD :: Annals of Dermatology
Novel association of neurofibromatosis type 1‐causing mutations in families with neurofibromatosis‐noonan syndrome - Ekvall - 2014 - American Journal of Medical Genetics Part A - Wiley Online Library
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
Multiple café-au-lait macules and movement disorder: think beyond neurofibromatosis
Chinese patient with neurofibromatosis-Noonan syndrome caused by novel heterozygous NF1 exons 1–58 deletion: a case report, BMC Pediatrics
Legius syndrome
Diagnostic difficulties and possibilities of NF1-like syndromes in childhood, BMC Pediatrics
Pediatric Dermatology Consult - December 2016
Legius Syndrome - an overview
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