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uniparental disomy of Chromosome 21
Also Known As:
Chromosome 21, uniparental disomy of; Mosaic trisomy 21; Uniparental disomy of 21
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Context: Research Results
Cells
Cellular Structures
Chromosomes
Mammalian Chromosomes
Human Chromosomes
21-22 and Y Human Chromosomes
Pair 21 Human Chromosomes
uniparental disomy of Chromosome 21
Genetic Phenomena
Genetic Structures
Chromosomes
Mammalian Chromosomes
Human Chromosomes
21-22 and Y Human Chromosomes
Pair 21 Human Chromosomes
uniparental disomy of Chromosome 21
Genetic Variation
Mutation
Chromosome Aberrations: 11361
Aneuploidy: 8932
Trisomy: 1642
uniparental disomy of Chromosome 21
Uniparental Disomy: 327
uniparental disomy of Chromosome 21
Chromosome Duplication: 167
Trisomy: 1642
uniparental disomy of Chromosome 21
Mosaicism
uniparental disomy of Chromosome 21
Ploidies
Aneuploidy: 8932
Trisomy: 1642
uniparental disomy of Chromosome 21
Signs and Symptoms Pathological Conditions
Pathologic Processes: 10023
Chromosome Aberrations: 11361
Aneuploidy: 8932
Trisomy: 1642
uniparental disomy of Chromosome 21
Chromosome Duplication: 167
Trisomy: 1642
uniparental disomy of Chromosome 21
Genetic Nondisjunction
Uniparental Disomy: 327
uniparental disomy of Chromosome 21