INIS
birth
18%
cancer
22%
carriers
30%
congenital diseases
13%
control
13%
data
16%
detection
16%
diseases
28%
dna
22%
drugs
15%
embryos
15%
erythrocytes
14%
genes
60%
genetics
100%
humans
30%
in vitro
11%
inosine
12%
levels
12%
mitochondria
11%
mutations
72%
nucleotides
12%
ovaries
12%
patients
52%
pregnancy
15%
risks
36%
screening
12%
spectra
14%
testing
42%
therapy
10%
weight
11%
Biochemistry, Genetics and Molecular Biology
Autosomal Recessive Disorder
6%
Birth Weight
10%
BRCA1
6%
Candidate Gene
6%
Carbohydrate Metabolism
6%
DNA Mutation
6%
Exome
6%
Exome Sequencing
8%
Gene Linkage
7%
Genetic Screening
25%
Genetics
29%
Genotyping
9%
Human Ether A Go Go Related Gene
9%
Human Immunodeficiency Virus
9%
Inorganic Pyrophosphatase
6%
Inosine
9%
Inosine Triphosphatase
12%
ITPA
7%
Leptin
8%
Lipid Metabolism
6%
Long QT Syndrome
15%
Mitochondrial DNA
10%
Mosaicism
9%
Penetrance
7%
Preimplantation
23%
Preimplantation Genetic Diagnosis
19%
PTCH1
6%
Single-Nucleotide Polymorphism
7%
Whole Genome Sequencing
6%
ZIC2
6%
Keyphrases
Basal Cell Nevus Syndrome
9%
Belgian
6%
Birth Weight
14%
Bladder Cancer
6%
Bladder Cancer Risk
6%
Consanguineous
9%
Erythrocytes
11%
Exome
6%
Flanders
10%
Genetic Diagnosis
6%
Haplarithmisis
7%
Hereditary Breast Cancer
6%
Hereditary Ovarian Cancer
6%
Heritability
6%
Holoprosencephaly
12%
Inosine Triphosphatase
12%
KCNH2
7%
Leptin
6%
Long QT Syndrome
13%
Metabolic Risk Factors
7%
Mitochondrial DNA mutation
6%
Mutation Carriers
6%
Netherlands
9%
Neurofibromatosis Type I
6%
Novel mutation
7%
Polymorphism
8%
Preimplantation Genetic Diagnosis
52%
Preimplantation Genetic Testing for Monogenic Disorders (PGT-M)
7%
PTCH1
6%
SCN5A
6%
