Legius Syndrome - an overview
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Figure 2 from Legius syndrome, an Update. Molecular pathology of mutations in SPRED1.
Neurofibromatosis Type 1: Practice Essentials, Background, Pathophysiology
Legius Syndrome - an overview
Rasopathies: Developmental Disorders That Predispose to Cancer and Skin Manifestations
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
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
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Legius syndrome
PDF] Clinical and mutational spectrum of neurofibromatosis type 1-like syndrome.
Children, Free Full-Text
Legius Syndrome - DoveMed
Café-au-lait macule differential by craniofacial examination. Many of
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