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QuickView for chromosomes human, pair 21
Most Correlated Studies
- OMIM - Congenital disorder
- Acute myeloid leukemia by karyotype and by discrete mutation
- Bone marrow gene expression of pediatric acute lymphoblastic leukemia
- Bone marrow or peripheral blood mononuclear cells of pediatric acute myeloid leukemia patients
- Bone marrows from acute myleoid leukemia (AML) patients grouped by chromosomal abnormalities
Most Relevant Literature
- Maternal uniparental disomy of chromosome 21 as a cause of pseudo-exclusion from paternity.
- Variegated overexpression of chromosome 21 genes reveals molecular and immune subtypes of Down syndr…
- DNA methylation correlation structure of chromosome 21 in Down syndrome.
- Extracellular chromosome 21--derived microRNAs in maternal circulation: evaluation of their diagnost…
- Global Repeat Map (GRM): Advantageous Method for Discovery of Largest Higher-Order Repeats (HORs) in…
Most Relevant Clinical Trials
- A Positional Cloning Study on Schizophrenia
- Molecular Genetic Study of Schizophrenia: Parent-Offspring Trios
- The Association Between Telomere Length and Propofol Dose in Anesthesia-induction
- Validation of the Accuracy of DNA Fingerprinting Using Polar Bodies and Embryonic Cells
- Automated Intracytoplasmic Sperm Injection (ICSIA)
