| Across |
| 3. | A test made in early pregnancy to detect congenital abnormalities in the fetus |
| 6. | The failure of homologous chromosomes to separate normally during nuclear division. |
| 7. | A threadlike structure of nucleic acids and protein found in the nucleus of most living cells |
| 10. | an indivicual that has one copy of a recessive allele that causes a genetic disease in individual that are homozygous for this allele |
| 11. | Alleles of an organism |
| 14. | The sampling of amniotic fluid using a hollow needle inserted into the uterus, to screen for developmental abnormalities in a fetus. |
| 16. | n allele that produces the same phenotype whether its paired allele is identical or different. |
| 18. | Showing a degree of similarity (e.g. in position, structure, function or characteristics) that may indicate a common origin. |
| 19. | A unit of heredity that is transferred from a parent to offspring |
| 20. | Having a single set of unpaired chromosomes |
| 21. | Containing two complete sets of chromosomes, one from each parent. |
| 22. | One of two or more alternative forms of a gene that arise by mutation and are found at the same place on a chromosome. |
| 23. | Any of a group of basic proteins found in chromatin |