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chromosome 21
Summary
General Info
Curated Studies
Most Correlated Studies
Monocytes and T cells from disomic and trisomic chromosome 21 subjects
OMIM - Congenital disorder
Acute myeloid leukemia by karyotype and by discrete mutation
Bone marrows from acute myleoid leukemia (AML) patients grouped by chromosomal abnormalities
Bone marrow or peripheral blood mononuclear cells of pediatric acute myeloid leukemia patients
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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…
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Most Relevant Clinical Trials
Trisomy of Chromosome 21 Diagnosis by High Output Sequencing
Non-Invasive Determination of Fetal Chromosome Abnormalities
Non Invasive Prenatal Diagnosis of Trisomy 21 by Genetic Analysis of Circulating Fetal Cells
Non-invasive Screening of Fetal Trisomy 21 by Digital PCR
Non-Invasive Chromosomal Evaluation of Trisomy Study
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