Medicine & Life Sciences
Neurofibromatosis 1
100%
Mutation
79%
Plexiform Neurofibroma
75%
Genes
50%
pirfenidone
48%
Neurofibroma
45%
Phenotype
43%
Neurofibromatoses
41%
Congenital Disorders of Glycosylation
39%
Intellectual Disability
33%
Neoplasms
30%
Child
27%
Whole Exome Sequencing
25%
Muscle Hypotonia
23%
Schwannomatosis
23%
Lipectomy
20%
Legius syndrome
20%
Mannose-6-Phosphate Isomerase
19%
Precision Medicine
19%
Chromosomes
18%
Mannose-Binding Protein Deficiency
17%
Pheochromocytoma
17%
Glycosylation
17%
Missense Mutation
17%
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
16%
Mosaicism
15%
Alleles
15%
Genetic Testing
15%
Mothers
15%
Cerebellar Ataxia
14%
Turner Syndrome
13%
Exons
12%
Megalencephaly
12%
Therapeutics
12%
Kennerknecht Sorgo Oberhoffer syndrome
12%
Growth
12%
Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip-Palate
11%
Magnetic Resonance Imaging
11%
Short chain Acyl CoA dehydrogenase deficiency
11%
Type 2 Oto-palato-digital syndrome
11%
Pulmonary Valve Stenosis
11%
Polyprenols
11%