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Congenital hyperthyroidism with reciprocal translocation t(1;17)(q25;q21)
M Gregori-Romero1, C López-Ginés, R Gil
1Department of Pathology, Faculty of Medicine, University of Valencia, Spain.
Human Genetics
|September 1, 1989
Summary
Researchers identified a rare 1;17 translocation in a patient. They are seeking collaboration with other scientists who have encountered similar chromosomal abnormalities.
Area of Science:
- Genetics
- Cytogenetics
- Human Genetics
Background:
- Chromosomal translocations are significant in genetic research.
- The 1;17 translocation is a specific type of chromosomal rearrangement.