Fragile chromosome 16(q22) cause a balanced translocation at the same point
| Autor: | C. San Román, M E Gallego Gómez, G Lledo, J.M. García-Sagredo |
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| Rok vydání: | 1983 |
| Předmět: |
Adult
Male Genetics Chromosome Fragile Sites Chromosome Fragility Chromosomal fragile site Chromosomal translocation Karyotype Biology medicine.disease Translocation Genetic Chromosome 16 Break point Chromosome Fragile Site Karyotyping Chromosome abnormality medicine Humans Child Genetics (clinical) Chromosomes Human 16-18 |
| Zdroj: | Human Genetics. 65:211-213 |
| ISSN: | 1432-1203 0340-6717 |
| DOI: | 10.1007/bf00286668 |
| Popis: | A father with a fragile 16(q22) has a son with a de novo balanced translocation 1;16. Both the fragile site and the break point at chromosome 16 are similar (q22). The question of whether the fragile site can cause a structural chromosome abnormality at the same point is discussed. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
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