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Trisomy 18-Like Syndrome
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Disease Context: Research Results
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
Congenital Abnormalities: 25723
Multiple Abnormalities: 211
Trisomy 18-Like Syndrome
Chromosome Disorders: 136
Trisomy 18-Like Syndrome
Inborn Genetic Diseases: 11939
Chromosome Disorders: 136
Trisomy 18-Like Syndrome
Cells
Cellular Structures
Chromosomes
Mammalian Chromosomes
Human Chromosomes
16-18 Human Chromosomes
Pair 18 Human Chromosomes
Trisomy 18-Like Syndrome
Genetic Phenomena
Genetic Structures
Chromosomes
Mammalian Chromosomes
Human Chromosomes
16-18 Human Chromosomes
Pair 18 Human Chromosomes
Trisomy 18-Like Syndrome
Genetic Variation
Mutation
Chromosome Aberrations: 11361
Aneuploidy: 8932
Trisomy: 1642
Trisomy 18-Like Syndrome
Chromosome Duplication: 167
Trisomy: 1642
Trisomy 18-Like Syndrome
Ploidies
Aneuploidy: 8932
Trisomy: 1642
Trisomy 18-Like Syndrome
Signs and Symptoms Pathological Conditions
Pathologic Processes: 10023
Chromosome Aberrations: 11361
Aneuploidy: 8932
Trisomy: 1642
Trisomy 18-Like Syndrome
Chromosome Duplication: 167
Trisomy: 1642
Trisomy 18-Like Syndrome