Biochemistry, Genetics and Molecular Biology
Mutation
100%
Preimplantation Genetic Diagnosis
54%
Nested Gene
52%
Spectrum
40%
COL4A5
36%
Pregnancy
35%
Genotype Phenotype Correlation
32%
Phenotype
29%
Mental Retardation
25%
Genetics
23%
Age
23%
Hearing
22%
Germline Mutation
21%
EZH2
21%
Whole Genome Sequencing
21%
Genetic Disorder
20%
Exon
18%
Birth
18%
Fluorescence in Situ Hybridization
15%
Incidence
15%
Body Height
14%
Gene Mutation
14%
Screening
12%
Health
12%
Collagen
11%
Probe
11%
Array Comparative Genomic Hybridization
10%
Single Gene Disorder
10%
Oncogene
10%
Microarray
10%
Height
10%
Chromosome 6p
10%
Robertsonian Translocation
10%
Reciprocal Chromosome Translocation
10%
Podocyte
10%
Mitochondrial DNA
10%
Germline
10%
Homeobox
10%
Loss of Heterozygosity
10%
Chromosome 5p
10%
Doublecortin
10%
Progeny
9%
Copy-Number Variation
9%
Development
9%
Population
9%
Comprehension
9%
Allele
8%
Myosin
7%
Chromosome 5
7%
Exome Sequencing
7%
Medicine and Dentistry
Preimplantation Genetic Diagnosis
54%
Patient
47%
Pregnancy
47%
Family
41%
Disease
31%
Gene
27%
Diagnosis
26%
Athletic Training
24%
Child
23%
Skin
22%
Rare Disease
21%
Syndrome
21%
Genetic Disorder
20%
Disability
20%
Obstetric Delivery
17%
National Health Service
15%
Chromosome Aberration
15%
Woman
15%
Spontaneous Abortion
15%
Genetic Screening
15%
Childbirth
14%
Male
14%
Health Care
14%
Prenatal Diagnosis
14%
Experience
13%
Adult
12%
Erythrocyte
12%
Exon
12%
Analysis
12%
Basement Membrane
11%
Psychiatry
10%
Down Syndrome
10%
Kabuki Syndrome
10%
Prospective Cohort Study
10%
Karyotype
10%
Tetraspanin
10%
Whole Genome Sequencing
10%
Microarray
10%
Narrative
10%
Diagnostics
10%
Robertsonian Chromosome Translocation
10%
Reciprocal Chromosome Translocation
10%
Chromosome 1
10%
Dandy Walker Syndrome
10%
Nephropathy
10%
Family Communication
10%
Primary Hyperparathyroidism
10%
Systematic Review
10%
Multiple Endocrine Neoplasia Type I
10%
Medicine
10%
