Medicine and Dentistry
Patient
100%
Syndrome
66%
Diagnosis
65%
Hereditary Nonpolyposis Colorectal Cancer
39%
Gene
36%
Family
35%
Adult
31%
Rokitansky Syndrome
27%
Malignant Neoplasm
25%
Diseases
25%
Colorectal Cancer
25%
Age
23%
Therapeutic Procedure
22%
Female
22%
Association
19%
Molar Pregnancy
18%
Inpatient
18%
DNA Mismatch Repair
16%
Hereditary Colorectal Cancer
16%
Peutz Jeghers Syndrome
16%
Epilepsy
16%
Follow up
15%
Case Report
13%
Cancer Risk
13%
Mortality
13%
Pregnancy
12%
Analysis
11%
Clinical Genetics
11%
Woman
11%
Hypophosphatasia
11%
Cancer Staging
11%
Salpingooophorectomy
11%
Polycystic Kidney Disease
11%
Hysterectomy
11%
Gestational Trophoblastic Disease
11%
Autosomal Dominant Inheritance
11%
Hypodontia
11%
Death
10%
Polyposis
10%
Genotype
10%
Hospital
10%
Colonoscopy
9%
Child
8%
Exome Sequencing
8%
Male
8%
Sensorineural Hearing Loss
8%
Complication
8%
Neoplasm
7%
Childbirth
7%
Girl
7%
Clinical Finding
7%
Counseling
7%
Cohort Analysis
7%
Etiology
7%
Organ
7%
Renal Cyst
6%
Prostate Cancer
6%
Laboratory
6%
Examination
6%
Cancer Susceptibility
6%
Personalized Medicine
6%
Cyst
6%
Vagina Aplasia
6%
Infertility
6%
Trophoblast
6%
Juvenile Polyposis Syndrome
6%
Clinical Management
6%
Skin
6%
Gender
6%
Epileptic Seizure
6%
Retrospective Cohort Study
5%
Hazard Ratio
5%
Disorders of Mitochondrial Functions
5%
Maternal Blood
5%
Lactic Acidosis
5%
Familial Disease
5%
Gene Repair
5%
Cancer Therapy
5%
Glucose
5%
Left Coronary Artery
5%
Genetic Disorder
5%
Arthrogryposis
5%
Marfan Syndrome
5%
Apoplexy
5%
Limb Defect
5%
Phosphate
5%
Nosology
5%
Megalin
5%
Elastin
5%
Hypoparathyroidism
5%
Maternal Welfare
5%
Dizziness
5%
Chondrodysplasia
5%
Overdiagnosis
5%
Telomere
5%
Sucrose
5%
Patient Characteristics
5%
Drusen
5%
Isoprenaline
5%
Ocular Albinism
5%
Biochemistry, Genetics and Molecular Biology
Gene
88%
Genetics
58%
Spectrum
40%
Missense
35%
Germline
29%
Exome Sequencing
28%
Genotyping
28%
DNA
22%
Preimplantation
22%
Cohort Study
17%
Bone
17%
Genome Sequencing
17%
Protein
15%
Case Report
14%
Microsatellite DNA
13%
Next Generation Sequencing
12%
Sequencing
12%
Trophoblast
12%
Genetic Disorder
12%
Cross Sectional Study
12%
MLH1
11%
Aneuploidy
11%
Phosphorylase
11%
Kinase
11%
Mental Retardation
11%
Genetic Counseling
8%
Candidate Gene
8%
Phosphate
7%
Bone Strength
6%
Genetic Predisposition
6%
X-Inactivation
6%
Gene Repair
6%
Exon
6%
Alkaline Phosphatase
5%
Quantitative Technique
5%
Wilms' Tumor
5%
Glucose
5%
Sucrose
5%
Homeobox
5%
Aggrecan
5%
X-Linked Recessive Inheritance
5%
HDAC8
5%
Factor H
5%
Trisomy 21
5%
FCGR2A
5%
TLR4
5%
Down Syndrome
5%
Parathyroid Hormone
5%
Chromosome 21 (Human)
5%
Gene Polymorphism
5%
Dermatan Sulfate
5%
Endopeptidase
5%
Type I Collagen
5%
Skewed X-Inactivation
5%
Trisomy
5%
PHKA2
5%
Leber's Hereditary Optic Neuropathy
5%
Angioedema
5%
Amino Acids
5%
Microphthalmia-Associated Transcription Factor
5%
Angiotensin-Converting Enzyme
5%
ATP Synthase
5%
Neuropathy, Ataxia, and Retinitis Pigmentosa
5%
Methylenetetrahydrofolate Reductase
5%
MT-ATP6
5%
Enzyme Inhibitor
5%
BAP1
5%
PMS2
5%