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Chromosomal Instability with Tissue-Specific Radiosensitivity
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Disease Context: Research Results
Musculoskeletal Diseases: 719
Musculoskeletal Abnormalities: 43
Craniofacial Abnormalities: 203
Microcephaly: 1471
Chromosomal Instability with Tissue-Specific Radiosensitivity
Nervous System Diseases: 14178
Nervous System Malformations: 35
Malformations of Cortical Development: 376
Group I Malformations of Cortical Development
Microcephaly: 1471
Chromosomal Instability with Tissue-Specific Radiosensitivity
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
Congenital Abnormalities: 25723
Musculoskeletal Abnormalities: 43
Craniofacial Abnormalities: 203
Microcephaly: 1471
Chromosomal Instability with Tissue-Specific Radiosensitivity
Nervous System Malformations: 35
Malformations of Cortical Development: 376
Group I Malformations of Cortical Development
Microcephaly: 1471
Chromosomal Instability with Tissue-Specific Radiosensitivity
Neoplasms: 1324753
Chromosomal Instability with Tissue-Specific Radiosensitivity
Signs and Symptoms Pathological Conditions
Pathologic Processes: 10023
Chromosome Aberrations: 11361
Chromosomal Instability: 2644
Chromosomal Instability with Tissue-Specific Radiosensitivity
Genomic Instability: 9619
Chromosomal Instability: 2644
Chromosomal Instability with Tissue-Specific Radiosensitivity
Genetic Phenomena
Genomic Instability: 9619
Chromosomal Instability: 2644
Chromosomal Instability with Tissue-Specific Radiosensitivity
Genetic Variation
Mutation
Chromosome Aberrations: 11361
Chromosomal Instability: 2644
Chromosomal Instability with Tissue-Specific Radiosensitivity