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Pitfalls in the use of chromosome variants for paternity dispute cases
- Source :
- Human genetics. 37(3)
- Publication Year :
- 1977
-
Abstract
- A huge ‘satellite’ (22s+) was observed in a mentally retarded and malformed girl. It consisted of constitutive heterochromatin based on the C-band technique (CBG). In neither of the parents was the variant observed. Genetic marker studies revealed that the father was, indeed, the father of the proposita (probability, 99.8%). It is emphasized that caution must be taken in the use of chromosome variants for paternity dispute cases.
- Subjects :
- Genetics
Chromosome Aberrations
Paternity
Mentally retarded
Biology
Human genetics
Chromosome (genetic algorithm)
Paternity dispute
Genetic marker
Child, Preschool
Heterochromatin
Intellectual Disability
Karyotyping
Constitutive heterochromatin
Humans
Abnormalities, Multiple
Female
Genetics (clinical)
Subjects
Details
- ISSN :
- 03406717
- Volume :
- 37
- Issue :
- 3
- Database :
- OpenAIRE
- Journal :
- Human genetics
- Accession number :
- edsair.doi.dedup.....57e8c64e05422f1b5714e2da490e3840