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Acute myeloid leukemia by karyotype and by discrete mutation
Chromosome 5q deletion in therapy-related myeloid neoplasms (t-MN)
B16F10 microcell hybrid cells carrying human chromosome 5 with and without telomerase activity
OMIM - Congenital chromosomal disease
OMIM - Congenital disorder
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Novel Concept of Alpha Satellite Cascading Higher-Order Repeats (HORs) and Precise Identification of…
A novel imprinted locus on bovine chromosome 18 homologous with human chromosome 16q24.1.
Chromosome-specific induction of micronuclei and chromosomal aberrations by mitomycin C: Involvement…
Higher-Order Structure of Human Chromosomes Observed by Electron Diffraction and Electron Tomography…
Inversions on human chromosomes.
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Generation of Haploid Stem Cells From Human Germ Cells
Reversing Epigenetic & Other Markers of Senescence by Transfusing Young Plasma To Older Human Subjec…
Genetic Study of Familial Epilepsy
Human Factors Study to Validate the User Interface of TOBI Podhaler Using Placebo Capsules
Sex Selection of Human Spermatozoa
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