INIS
phenotype
100%
genes
100%
variations
99%
tumors
74%
breasts
74%
translocation
74%
mutations
74%
chromosomes
74%
downs syndrome
74%
abnormalities (chromosomal)
74%
humans
74%
diseases
74%
biology
74%
defects
74%
patients
62%
codons
50%
malformations
43%
segregation
37%
meiosis
37%
angiogenesis
37%
children
37%
gametes
37%
genetics
37%
philadelphia chromosome
37%
amenorrhea
37%
obstetrics
37%
genesis
37%
residues
24%
comparative evaluations
24%
tryptophan
24%
tissues
24%
congenital diseases
24%
dna
24%
holes
24%
genotype
24%
follicle stimulating hormone
24%
x chromosome
24%
cancer
24%
cadmium 105
24%
walls
24%
exons
24%
tropomyosin
18%
accounting
18%
receptors
12%
physiology
12%
chaos theory
12%
screens
12%
proliferation
12%
management
12%
antineoplastic drugs
12%
Medicine and Dentistry
Cytotechnology
74%
Endothelial Cell
74%
Filamin
74%
Turner Syndrome
74%
Breast Tumor
74%
Disease Course
74%
Biological Product
74%
47,XXX Syndrome
74%
Prematurity
74%
Patient Referral
74%
Spontaneous Abortion
74%
Restrictive Cardiomyopathy
74%
Culture
44%
Patient
44%
Cells
44%
Angiogenesis
44%
Western Blot
44%
Primary Amenorrhea
37%
Recurrent Miscarriage
37%
Chromosome 4
37%
Karyotype
33%
Disease Exacerbation
29%
Phenotype
29%
Breast
29%
Antiangiogenic
29%
Reverse Transcription Polymerase Chain Reaction
29%
Gene
29%
Prognosis
29%
Cell Type
29%
Neoplasm
29%
Follitropin
24%
Hormone Determination
24%
X Chromosome
24%
Cardiac Shunt
24%
Heart Development
24%
Stop Codon
24%
Male Pseudohermaphroditism
24%
Mixed Gonadal Dysgenesis
24%
True Hermaphroditism
24%
Female Pseudohermaphroditism
24%
Chromosome 14
18%
Mosaicism
18%
Monosomy X
18%
XY Gonadal Dysgenesis
18%
Short Stature
18%
Chromosome 12
18%
Genetic Counseling
18%
Blood Culture
18%
Genetic Disorder
14%
Malignant Neoplasm
14%
Biochemistry, Genetics and Molecular Biology
Phenotype
89%
TBX5 (Gene)
74%
TPM1
74%
Case Report
74%
Filamin
74%
Mental Retardation
74%
Turner Syndrome
74%
Nonsense Mutation
74%
Chromosomal Abnormalities
56%
Body Height
37%
Down Syndrome
37%
Philadelphia Chromosome
37%
Chromosome 4
37%
Tryptophan
24%
Codon
24%
Stop Codon
24%
Genotyping
24%
Inheritance
24%
Autosomal Trisomies
24%
DNA
24%
Development
24%
Chromosome Abnormality
24%
Exon
24%
Triple X Syndrome
18%
Inversion
18%
Monosomy
18%
X Chromosome
18%
Chromosome 12
18%
Prevalence
18%
Genetic Counseling
18%
Karyotyping
18%
Receptor Antagonist
14%
Endoglin
14%
Sorafenib
14%
Endothelial Progenitor Cell
14%
Anticoagulation
14%
Stable Expression
14%
VE-cadherin
14%
Life
14%
Genetic Disorder
14%
Genetic Background
14%
Genetic Screening
14%
Nested Gene
14%
Tropomyosin
12%