Biochemistry, Genetics and Molecular Biology
Klinefelter Syndrome
100%
Comorbidity
60%
Biochemistry
56%
Insulin Resistance
52%
Turner Syndrome
50%
Hormonal Regulation
50%
Deceleration
50%
Cross Sectional Study
50%
Transforming Growth Factor Beta
50%
TIMP1
50%
Hypercalciuria
50%
XYY Syndrome
50%
Blood Pressure
50%
Glucocorticoid
50%
Insulin Sensitivity
50%
Electrocardiogram
50%
Autosomal Recessive Disorder
50%
Cortisol
50%
Lipid
50%
Karyotype 47,XXY
20%
Sex Chromosome
20%
Kidney Function
18%
Calcium Excretion
12%
Liver Function
12%
Genetics
10%
Medline
10%
Problem Behavior
10%
Y Chromosome
10%
Matrix Metalloproteinase
8%
Heterozygosity
8%
Alanine
7%
Transaminase
7%
Urine Sampling
6%
Prevalence
6%
Parathyroid Hormone
6%
Cholesterol Blood Level
5%
Principal Component Analysis
5%
Medicine and Dentistry
Klinefelter Syndrome
100%
Cross Sectional Study
50%
Hypoparathyroidism
50%
Hypercalciuria
50%
Nephrocalcinosis
50%
Congenital Malformation
50%
Turner Syndrome
50%
Congenital Adrenal Hyperplasia
50%
47,XYY Syndrome
50%
Transforming Growth Factor Beta
50%
Abdominal Obesity
50%
Mild Hepatic Impairment
50%
Early Diagnosis
20%
47,XXY Syndrome
20%
Kidney Function
18%
Cardiovascular Risk
16%
Anthropometry
15%
Quality of Life
15%
Biological Marker
15%
Calcium Excretion
12%
Liver Function
12%
Organ Systems
10%
Counseling
10%
Y Chromosome
10%
Disease
10%
Problem Behavior
10%
Chromosome Disorder
10%
Early Intervention
10%
Neonatal Infant
10%
Cardiovascular System
10%
Metabolic Syndrome
10%
Sex Chromosome
10%
Body Mass Index
10%
Cardiovascular Disease
8%
Biochemical Marker
8%
Heterozygosity
8%
Matrix Metalloproteinase
8%
Alanine Aminotransferase
7%
Adverse Event
6%
Prevalence
6%
Chronic Kidney Disease
6%
Urine Sampling
6%
Calcium Ion
6%
Parathyroid Hormone
6%
Adrenal Cortex
5%
Autosomal Recessive Disorder
5%
Blood Pressure
5%
Hormonal Regulation
5%
Hyperandrogenism
5%
Glucocorticoid
5%
