Medicine & Life Sciences
Turner Syndrome
100%
X Chromosome
50%
Phenotype
50%
Primary Ovarian Insufficiency
44%
Leri-Weil syndrome
42%
Genes
40%
Klinefelter Syndrome
34%
Germ Cells
31%
Haploinsufficiency
30%
Cyclin A1
29%
Langer mesomelic dysplasia
25%
Sex Chromosomes
25%
Mutation
21%
Obesity
20%
T-Lymphocytes
20%
Receptor, Melanocortin, Type 4
19%
Meiosis
18%
Homeobox Genes
18%
Introns
17%
X Chromosome Inactivation
17%
Yeasts
17%
Sperm Capacitation
17%
ribosomal protein S4
16%
Cryptococcosis
16%
21S rRNA
16%
Y Chromosome
16%
Cytokines
16%
Gametogenesis
16%
XYY syndrome 47
15%
Cyclin A
15%
Cyclin A2
14%
Melanocortins
14%
Gene Dosage
14%
Paraventricular Hypothalamic Nucleus
13%
Oxytocin
13%
Cryptococcus neoformans
13%
Th2 Cells
13%
Helper-Inducer T-Lymphocytes
12%
lipid transfer protein
12%
Cell Cycle Checkpoints
12%
Spermatogenesis
12%
B-Lymphocytes
12%
Cell Cycle
11%
Interleukin-4 Receptors
11%
Interleukin-4
11%
Lung
11%
Testis
11%
Follicular Fluid
10%
Th1 Cells
10%
Neurons
10%
Flagellin
10%
Haploidy
10%
Antigens
10%
Pigmentary Disorder, Reticulate, with Systemic Manifestations
10%
Turner Syndrome-Associated Neurocognitive Phenotype
9%
Clone Cells
9%
B-Cell Lymphoma
9%
Anti-Idiotypic Antibodies
9%
Y-Linked Genes
9%
Karyotype
9%
T-Lymphocyte Epitopes
9%
DNA
9%
Hypospadias
9%
Chromosomes, Human, Pair 13
8%
Sex Chromosome Disorders
8%
Proteins
8%
Inbred C57BL Mouse
8%
Interferons
8%
X-Linked Genes
8%
Anorexia
8%
Arrest of spermatogenesis
8%
Cognition
8%
Oocytes
8%
Gene Silencing
8%
Autistic Disorder
8%
Salmonella
8%
Hyperphagia
8%
SCID Mice
8%
Interleukin-5
7%
Congresses
7%
Ovary
7%
monoclonal antibody GK1.5
7%
Pseudoautosomal Regions
7%
Transgenes
7%
human PLTP protein
7%
Messenger RNA
7%
Psychological Imprinting
7%
Growth
7%
Child
7%
Cleavage Stimulation Factor
7%
VACTERL association
7%
Mothers
7%
Penoscrotal transposition
7%
Natural Killer Cells
7%
Hypothalamus
7%
Chromosome Aberrations
7%
Cyclin H
6%
rRNA Genes
6%
Protein Isoforms
6%
Heterozygote
6%