Medicine & Life Sciences
Neurofibromatosis 1
100%
Mutation
80%
Plexiform Neurofibroma
74%
Genes
51%
pirfenidone
47%
Phenotype
46%
Neurofibroma
44%
Neurofibromatoses
41%
Congenital Disorders of Glycosylation
38%
Intellectual Disability
33%
Neoplasms
30%
Child
28%
Whole Exome Sequencing
25%
Muscle Hypotonia
23%
Schwannomatosis
22%
Lipectomy
20%
Legius syndrome
19%
Mannose-6-Phosphate Isomerase
19%
Precision Medicine
18%
Chromosomes
18%
Mannose-Binding Protein Deficiency
17%
Exome
17%
Pheochromocytoma
17%
Glycosylation
17%
Missense Mutation
16%
Fluorescence In Situ Hybridization
16%
Smith-Lemli-Opitz Syndrome
16%
Neurilemmoma
16%
Ornithine Carbamoyltransferase Deficiency Disease
16%
Butyryl-CoA Dehydrogenase
16%
Dolichols
16%
Neurofibromatosis 2
16%
Genetic Association Studies
15%
Mosaicism
15%
Alleles
15%
Mothers
15%
Genetic Testing
14%
Neurofibrosarcoma
14%
Cerebellar Ataxia
14%
Megalencephaly
13%
Turner Syndrome
13%
Exons
12%
Therapeutics
12%
Kennerknecht Sorgo Oberhoffer syndrome
11%
Growth
11%
Translational Medical Research
11%
Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip-Palate
11%
Magnetic Resonance Imaging
11%
Short chain Acyl CoA dehydrogenase deficiency
11%