Keyphrases
Spermatozoa
100%
Interchromosomal Effect
64%
Fluorescence in Situ Hybridization
55%
MicroRNA
55%
Gametes
35%
Male Infertility
31%
Robertsonian Translocation
30%
Reciprocal Translocation
30%
Human Sperm
29%
Human Spermatozoa
25%
Segregation Patterns
25%
In Situ Hybridization
24%
Chromosome Abnormalities
23%
Meiotic Behavior
23%
Translocation Carrier
23%
Structural Reorganization
19%
Quantitative PCR
18%
Sperm nuclei
18%
Homologous Chromosomes
17%
Chromosome Positioning
17%
Spermatogenesis
17%
Segregation Effect
17%
Segregation Analysis
16%
Chromosome Y
16%
Duplication
14%
Pericentric Inversion
14%
Expression Profile
14%
Semen Samples
14%
Chromosome 18
14%
Sperm FISH
14%
Reproductive Risk
13%
Low-copy Repeats
13%
Normozoospermic
12%
Non-coding RNA (ncRNA)
11%
Disomy
11%
Germ Cells
11%
Fertility Biomarkers
10%
Effect Analysis
10%
Sperm RNA
10%
Numerical Anomaly
10%
Chromosome 13
10%
Non-homologous Recombination
10%
Recombination
10%
American Society
10%
Reproductive Medicine
10%
Sex Chromosomes
9%
Chromosome X
9%
Meiosis
9%
Chromosomal Abnormalities
9%
Differentially Expressed mRNAs (DEmRNAs)
9%
Biochemistry, Genetics and Molecular Biology
Fluorescence in Situ Hybridization
85%
MicroRNA
55%
RNA
48%
Germ Cell
41%
Genetics
33%
Reciprocal Chromosome Translocation
31%
Robertsonian Translocation
31%
Male Fertility
29%
Chromosome Abnormality
22%
Spermatogenesis
20%
Sex Chromosome
19%
Y Chromosome
18%
Homologous Chromosome
17%
Chromosome Positioning
17%
Reproduction
16%
Cytogenetics
16%
Chromosome 18
16%
Low Copy Repeats
13%
Synapsis
13%
Disomy
13%
Chromosome 13
12%
Gene Expression
12%
Non-Allelic Homologous Recombination
11%
Real-Time Polymerase Chain Reaction
11%
Karyotype
10%
Chromosomal Abnormalities
10%
Chromosome 21
10%
X Chromosome
10%
Meiosis
9%
Quantitative Reverse Transcription Polymerase Chain Reaction
8%
Embryogenesis
8%
Genetic Carrier
8%
Dysplasia
8%
P21
8%
Heterozygote
8%
Long Non-Coding RNA
8%
Gene Activity
8%
Chromosome Inactivation
8%
Prader-Willi Syndrome
8%
TaqMan
8%
Biological Phenomena and Functions Concerning the Entire Organism
7%
Genetic Counseling
7%
Chromatid
7%
Chromosome 14
6%
Chromosome Rearrangement
6%
Progeny
6%
Pachytene
6%
Haplotype
6%
Genomics
6%
Population
5%
