Legius Syndrome - an overview
Por um escritor misterioso
Descrição
Café-Au-Lait Macules and Macrocephaly in a 19-Month-Old: Diagnostic Considerations Beyond Neurofibromatosis – Consult QD
Costello syndrome: a Ras/mitogen activated protein kinase pathway syndrome (rasopathy) resulting from HRAS germline mutations
Cureus, Neurofibromatosis-Noonan Syndrome With Primary Amenorrhoea: A Case Report
SPRED1 mutations (Legius syndrome): another clinically useful genotype for dissecting the neurofibromatosis type 1 phenotype
New research may help differentiate similar diagnoses - Levenson - 2010 - American Journal of Medical Genetics Part A - Wiley Online Library
Children, Free Full-Text
NF2 Information & Services - NF Month: Neurofibromatosis: Cafe Spots (CALMS Fact Sheet 12 #NF #NF1 #NF2 #NF3 #SWN #Neurofibromatosis #NFMonth2018 #NFAwarenessMonth Café-au-lait Marks (CALMS) or simply
Pediatric Dermatology Consult - December 2016
Noonan Syndrome with Multiple Lentigines - StoryMD
Cutaneous Expression of Familial Cancer Syndromes, HTML
de
por adulto (o preço varia de acordo com o tamanho do grupo)