Medicine & Life Sciences
Genes
100%
Exome
92%
Whole Exome Sequencing
90%
Phenotype
81%
Mutation
60%
Genetic Databases
48%
Intellectual Disability
46%
Siblings
46%
Genome
42%
Genomics
37%
Strudwick syndrome
35%
High-Throughput Nucleotide Sequencing
31%
Information Dissemination
28%
Scoliosis
24%
Databases
24%
Genetic Association Studies
23%
Microcephaly
23%
Kabuki syndrome
22%
Research Personnel
21%
lamin B receptor
20%
Proteins
20%
Zebrafish
20%
Muscle Hypotonia
18%
Alleles
17%
Enchondromatosis
17%
Inborn Genetic Diseases
17%
Penetrance
16%
Cleft Palate
16%
Hearing Loss
16%
Arrhythmogenic Right Ventricular Dysplasia
16%
HEM dysplasia
16%
Exons
15%
Fibroblasts
15%
Developmental Bone Disease
14%
Extremities
14%
Taurodontism, microdontia, and dens invaginatus
14%
Megacystis microcolon intestinal hypoperistalsis syndrome
14%
Nasopalpebral lipoma coloboma syndrome
13%
Pseudoaminopterin syndrome
13%
Peripheral Cone Dystrophy
13%
Scalp ear nipple syndrome
13%
Human Genome
13%
Myopathy, congenital nonprogressive with Moebius and Robin sequences
13%
Marden Walker like syndrome
12%
sphingolipid desaturase
12%
Mosaicism
12%
Coloboma
12%
Lateral meningocele syndrome
12%
Aniridia cerebellar ataxia mental deficiency
12%