Biochemistry, Genetics and Molecular Biology
Intellectual Disability
57%
Missense
43%
Prevalence
42%
Genetics
35%
SLC6A8
31%
Proband
31%
SMARCA2
30%
Genotyping
27%
Mouse
26%
Body Height
23%
Microdeletion Syndrome
21%
Genotype Phenotype Correlation
19%
Exome Sequencing
18%
Problem Behavior
16%
Allele
13%
Genetic Divergence
13%
Coding Region
13%
CDH2
12%
Bone Morphogenetic Protein 4
12%
Genetic Evaluation
12%
TUBB3
12%
Rett Syndrome
12%
EP300
12%
Mitochondrial Disorder
12%
PAX6
12%
Williams Syndrome
12%
Bovine Somatotropin
12%
Growth Hormone
12%
Mitogen-Activated Protein Kinase
12%
Structure Analysis
12%
Developmental Stage
12%
Syndrome Delineation
12%
Choline Transporter
12%
Indel
12%
Point Mutation
12%
Single-Nucleotide Polymorphism
12%
Actin
12%
DNA Methylation
12%
FOXP1
12%
Protein-Protein Interaction
12%
LMX1B
12%
Facial Recognition
12%
Rural Population
12%
Granulocyte
12%
NLRP7
12%
Protein Interaction
12%
Orthology
12%
Gene Interaction
12%
Histone Acetyltransferase
12%
GATA4
12%
Medicine and Dentistry
Fetal Alcohol Syndrome
100%
Prevalence
41%
Pediatrics
26%
Disease
19%
Neoplasm
15%
Brachycephaly
14%
Philtrum
13%
Genetic Disorder
13%
Peters Anomaly
13%
Diagnosis
12%
Dysmorphology
12%
Glycogen Storage Disease Type II
12%
Immune Deficiency
12%
Randomized Clinical Trial
12%
Bone Marrow Biopsy
12%
Clinical Guideline
12%
Haploinsufficiency
12%
Sepsis
12%
Glaucoma
12%
Open Angle Glaucoma
12%
Phakomatosis
12%
CYP1B1
12%
Hepatocyte Nuclear Factor 1
12%
Nephropathy
12%
Noonan Syndrome
12%
Clinical Management
12%
Cerebrospinal Fluid
12%
Partial Trisomy 9
12%
Partial Trisomy
12%
Hallux
12%
Whole Genome Sequencing
12%
Drug Exposure
12%
Anthrax Toxin
12%
Systemic Hyalinosis
12%
Bone Marrow Examination
12%
Cerebrospinal Fluid Culture
12%
Congenital Amegakaryocytic Thrombocytopenia
12%
Globoid Cell Leukodystrophy
12%
Ectodermal Dysplasia
12%
Synostosis
12%
Down Syndrome
12%
Hepatoblastoma
12%
Genetic Counseling
12%
Oppositional Disorder
12%
Eyebrow
12%
Developmental Coordination Disorder
12%
Speech Sound Disorder
12%
Speech Delay
12%
Leukocyte Adhesion Deficiency
10%
Congenital Malformation
9%
Keyphrases
Facial Analysis Technology
16%
Philtrum
14%
Peters Anomaly
12%
ACTG1
12%
Baraitser-Winter Syndrome
12%
Immunodeficiency
12%
Creatine Transporter Deficiency
12%
ZC4H2
12%
Arthrogryposis multiplex Congenita
12%
Computer-aided Recognition
12%
Antigen Test
12%
Peters Plus Syndrome
12%
Wiedemann-Steiner Syndrome
12%
B3GALTL
12%
Congenital Amegakaryocytic Thrombocytopenia
12%
Cryptococcus
12%
Van Den Ende-Gupta Syndrome
12%
RhGAA
12%
Neoplasms
12%
Syndrome Delineation
12%
Choline Transporter
12%
Tolerance Approach
12%
Pompe Disease
12%
P450 Oxidoreductase Deficiency
12%
Sepsis
12%
Escobar Syndrome
12%
Recessive Variants
12%
Facial Phenotyping
12%
Diverse Populations
12%
DeepGestalt
12%
DNA Methylation Signature
12%
Clinical Practice Guidelines
12%
Cerebrospinal Fluid
12%
Genetic Interaction Network
12%
Balanced Chromosomal Abnormalities
12%
Cryptococcus Neoformans
12%
Cryptococcal Infection
12%
Leukocyte Adhesion Deficiency
12%
KHDC3L
12%
Hyperadhesion
12%
NLRP7
12%
C6orf221
12%
Partial Trisomy 9
12%
Blood Fluid
12%
Offending
12%
Hyalinosis
12%
SLC25A46
12%
Anthrax Toxin Receptor 2 Gene
12%
Spectrum Disorder
12%
THOC6
12%