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Journal Article
Reproductive BioMedicine Online, ISSN 1472-6483, 01/2019, Volume 38, Issue 1, pp. 46 - 55
Chromosomal translocations are known genetic causes of male infertility. Are certain translocations or chromosomal regions more directly associated with sperm... 
Semen quality | Chromosomal translocation | Male infertility | Karyotype | ANOMALIES | RECIPROCAL TRANSLOCATIONS | CYTOGENETICS | MEIOTIC ASSOCIATION | OBSTETRICS & GYNECOLOGY | MALE-INFERTILITY | INACTIVATION | REPRODUCTIVE BIOLOGY | MEN | BREAKPOINT | XY-CHROMOSOMES | SPERM INJECTION
Journal Article
Journal Article
Medicine, ISSN 0025-7974, 03/2019, Volume 98, Issue 9, p. e14730
For genetic counseling of male carriers of chromosomal translocations, the specific chromosomes and breakpoints involved in the translocation are relevant to... 
genetic counseling | MEDICINE, GENERAL & INTERNAL | SPERM | GENE | ABNORMALITIES | SPERMATOZOA | RECIPROCAL TRANSLOCATION | SEGREGATION | male infertility | non-Robertsonian translocation | CARRIER | breakpoint
Journal Article
Frontiers in Genetics, ISSN 1664-8021, 01/2020, Volume 10
Chromosomal rearrangements have long fascinated evolutionary biologists for being widely implicated in causing genetic differentiation. Suppressed... 
Genetic markers | Chromosomes | Amphibians | Genetic polymorphisms | spiny frog | chromosomal rearrangement | recombination suppression | reciprocal translocation | hybrid unfitness
Journal Article
Human Mutation, ISSN 1059-7794, 02/2017, Volume 38, Issue 2, pp. 180 - 192
ABSTRACT Most balanced translocations are thought to result mechanistically from nonhomologous end joining or, in rare cases of recurrent events, by nonallelic... 
balanced chromosomal aberration | whole‐genome sequencing | reciprocal translocation | nonhomologous end joining | microhomology | replication‐based repair mechanisms | replication-based repair mechanisms | whole-genome sequencing | DIAGNOSIS | COMPLEX | REARRANGEMENTS | BREAKPOINTS | DELETION | INTELLECTUAL DISABILITY | ALIGNMENT | GENETICS & HEREDITY | ARCHITECTURE | MUTATIONS | RECEPTORS | Translocation, Genetic | Genetic Association Studies | Humans | Genotype | Homologous Recombination | In Situ Hybridization, Fluorescence | Male | Chromosome Mapping | DNA Copy Number Variations | Whole Genome Sequencing | Phenotype | Comparative Genomic Hybridization | Base Sequence | Female | Genomics - methods | Chromosome Breakage | Karyotype | Tourette's syndrome | Analysis | Genes | Genomics | Genetic research | Genetic aspects | Genomes | Nucleotide sequencing | DNA sequencing | whole genome sequencing | non-homologous end joining | Medical Biotechnology | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinsk bioteknologi | Medical Biotechnology (with a focus on Cell Biology (including Stem Cell Biology), Molecular Biology, Microbiology, Biochemistry or Biopharmacy) | Medicinsk bioteknologi (med inriktning mot cellbiologi (inklusive stamcellsbiologi), molekylärbiologi, mikrobiologi, biokemi eller biofarmaci)
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 01/2020, Volume 106, Issue 1, pp. 41 - 57
Unexplained infertility affects 2%–3% of reproductive-aged couples. One approach to identifying genes involved in infertility is to study subjects with this... 
balanced reciprocal translocation | meiosis | molecular cytogenetics | reproductive genetics | male infertility | topologically associating domain | CLINICAL VALIDITY | CHROMOSOME REARRANGEMENTS | PROTEIN | GENE-DISEASE ASSOCIATIONS | PROXIMITY-LIGATION | GERM-CELLS | GENETICS & HEREDITY | SYNAPTONEMAL COMPLEX | AZOOSPERMIA | R-CADHERIN | GENOME BROWSER
Journal Article