Biochemistry, Genetics and Molecular Biology
Nested Gene
100%
Chromosome 18
76%
Phenotype
76%
Chromosome
55%
Array Comparative Genomic Hybridization
33%
Growth Hormone
28%
Age
28%
Hemizygosity
24%
Chromosome Abnormality
23%
Genetics
22%
Penetrance
20%
Chromosome 18q
19%
Fluorescence in Situ Hybridization
17%
Cytogenetics
17%
Genotyping
17%
DNA
17%
Hearing
15%
Autosome
15%
Comprehension
15%
Incidence
15%
Candidate Gene
14%
Exercise
14%
Mental Retardation
13%
Copy-Number Variation
13%
Time
13%
Genotype Phenotype Correlation
13%
Karyotype
11%
Electric Potential
11%
Motivation
11%
Mutation
11%
Growth
11%
Clinical Trial
10%
TCF4
10%
Gene Expression
10%
Ring Chromosome
10%
Haploinsufficiency
9%
Osteolysis
9%
Gene Dosage
8%
Pedigree
8%
Bone
8%
Gene Mapping
8%
Myelination
7%
Case Report
7%
Birth
7%
Linkage Analysis
7%
Spectrum
7%
Inheritance
7%
Dicentric Chromosome
6%
X Chromosome
6%
Autosomal Recessive Inheritance
6%
Medicine and Dentistry
Gene
46%
Syndrome
44%
Child
43%
Chromosome 18
40%
Tetrasomy
28%
Phenotype
26%
Patient
24%
Growth Hormone
24%
Chromosome Aberration
17%
Arm
16%
Diseases
15%
Hearing Impairment
14%
Myelin Deficiency
14%
Paget's Disease
13%
Age
13%
Brain
12%
Growth Hormone Deficiency
12%
Growth
11%
Chromosome
10%
Sensorineural Hearing Loss
10%
Family
10%
Chromosome 18q
9%
Osteolysis
9%
Clinician
9%
Symptom
9%
Ear
8%
Corpus Callosum
8%
Myelination
8%
Strabismus
7%
Diagnosis
7%
Developmental Delay
7%
Hemizygosity
7%
Microarray Analysis
6%
Facioscapulohumeral Muscular Dystrophy
6%
Gene Expression
6%
Penetrance
6%
Dental Caries
6%
Stenosis
6%
Intelligence Quotient
6%
Growth Disorder
6%
Kidney Malformation
6%
Clinical Research
6%
Myelin
5%
Examination
5%
Analysis
5%
Motivation
5%
Comprehension
5%
Therapeutic Procedure
5%
Clinical Finding
5%
Evaluation Study
5%
