Results 181 to 190 of about 25,083,649 (268)
KIR2DL5 mutation and loss underlies sporadic dermal neurofibroma pathogenesis and growth [PDF]
Anastasaki, Corina +2 more
core +3 more sources
Oncogenetic testing, diagnosis and follow-up in Birt-Hogg-Dubé syndrome, familial atypical multiple mole melanoma syndrome and neurofibromatosis 1 and 2 [PDF]
't Kint de Roodenbeke, Daphné +13 more
core
Correction: Protein domain-specific genotype-phenotype correlation study of neurofibromatosis type 1. [PDF]
Ou M +7 more
europepmc +1 more source
Functional analysis of neurofibromatosis 2 (NF2) missense mutations.
D. Gutmann, A. Hirbe, C. Haipek
semanticscholar +1 more source
Hepatic plexiform neurofibroma a rare manifestation of neurofibromatosis type 1: A case report and literature review. [PDF]
Alkhaja OY +4 more
europepmc +1 more source

