Legius Syndrome - an overview
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PDF] Legius syndrome, an Update. Molecular pathology of mutations in SPRED1.
Frontiers Case Report: Sequential postzygotic HRAS mutation and gains of the paternal chromosome 11 carrying the mutated allele in a patient with epidermal nevus and rhabdomyosarcoma: evidence of a multiple-hit mechanism
What are RASopathies? – All About Cardiovascular System and Disorders
New research may help differentiate similar diagnoses - Levenson - 2010 - 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
Hong Kong Journal of Paediatrics [HK J Paediatr (New Series) 2018;23:294-297]
Neurofibromatosis Type 1: Practice Essentials, Background, Pathophysiology
Syndromes The RASopathies Network
Legius syndrome: case report and review of literature, Italian Journal of Pediatrics
Noonan Syndrome with Multiple Lentigines - StoryMD
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
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