Chromosome 21
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- Trisomy 21 - Down Syndrome
- Mosaic Down's Syndrome with De Novo 45,XX,-21, 22,+T(21Q;22Q)/46, XX,-21 ,+T(21Q;21Q) Rearrangement on September 30, 2021 by Guest
- Mutational Spectrum of CENP-B Box and Α-Satellite DNA on Chromosome 21 in Down Syndrome Children
- Extreme Reduction of Chromosome-Specific Α-Satellite Array Is Unusually Common in Human Chromosome 21
- Robertsonian Translocations T(21Q;21Q) and T(14Q;21Q) in Down Syndrome V
- The DNA Sequence of Human Chromosome 21
- Chromosome 21 Introduction Chromosome 21 Is an Acrocentric Chromosome. It Means That All of the Genes Are Located in the Long Ar
- Centromeres Under Pressure: Evolutionary Innovation in Conflict with Conserved Function
- Common Genetic Signatures of Alzheimer's Disease in Down
- Discovery of 33Mer in Chromosome 21 – the Largest Alpha Satellite Higher
- Applications of Genome Editing Technology in Research on Chromosome Aneuploidy Disorders
- How Does Down Syndrome Occur?
- A Physical Map of the Short Arm/Centromere Region of Human Chromosome 21
- Slightly Deleterious Genomic Variants and Transcriptome Perturbations in Down Syndrome Embryonic Selection
- Explaning Test Results/Karyotypes to Parents
- Chromosome 21
- Recounting a Genetic Story Roger H
- Consequences of Aneuploidy in Human Fibroblasts with Trisomy 21