Familial balanced insertion (5;10) and monosomy and trisomy (10) (q24.2----q25.3)
Autor: | M. J. Timmerman, M. F. Peters-Slough, A. Hagemeijer, M. J. van de Vooren, H. T. Planteydt |
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Rok vydání: | 1984 |
Předmět: |
Male
Monosomy Chromosome Disorders Trisomy Biology Translocation Genetic Meiosis Intellectual Disability Genetics medicine Humans Abnormalities Multiple Insertion Chromosomes Human 4-5 Genetics (clinical) Chromosomes Human 16-18 Chromosome Aberrations Chromosomes Human 6-12 and X Chromosome Fragility Chromosome Infant medicine.disease Phenotype Pedigree Three generations Chromosome Deletion |
Zdroj: | Clinical genetics. 25(1) |
ISSN: | 0009-9163 |
Popis: | The phenotype of a boy with monosomy of a small segment of chromosome (10) (q24.2----q25.3) is described. In his family a balanced insertion (5;10) is found in three generations. Moreover there are two persons who are trisomic for the same small segment of chromosome 10 for which the boy is monosomic. |
Databáze: | OpenAIRE |
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