Legius Syndrome - an overview
Por um escritor misterioso
Descrição
An Update on Neurofibromatosis Type 1: Not Just Café-au-Lait Spots, Freckling, and Neurofibromas. An Update. Part I. Dermatological Clinical Criteria Diagnostic of the Disease
PDF) Legius syndrome
Cureus, Neurofibromatosis-Noonan Syndrome With Primary Amenorrhoea: A Case Report
2023.03.05 Questions 34-35 - by Daniel Piqué
Genetic basis of neurofibromatosis type 1 and related conditions, including mosaicism
Noonan Syndrome with Cyanotic Congenital Heart Disease
Figure 1 from SPRED 1 Mutations in a Neurofibromatosis Clinic
Clinical features in 14 families with Legius syndrome
Noonan syndrome: improving recognition and diagnosis
Diagnostic difficulties and possibilities of NF1-like syndromes in childhood, BMC Pediatrics
Café-Au-Lait Macules and Macrocephaly in a 19-Month-Old: Diagnostic Considerations Beyond Neurofibromatosis – Consult QD
Genetic Clinics
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