Part,  Chapter, Paragraph

1   II,     5. 15.  3|           usually due to a single mutation segregating in family members.
2   II,     5. 15.  3|          are heterozygote for the mutation although healthy. Only 25%
3   II,     5. 15.  3|         children carry the double mutation which causes the disease.
4   II,     5. 15.  3|          carry the same recessive mutation, especially for very rare
5   II,     9        | attributed to a known single gene mutation, and under 5% to exposure
6   II,     9.  1.  2| attributed to a known single gene mutation, and under 5% to exposure
7  III,    10.  2.  4|        are often both disease and mutation specific. European networks
8  III,    10.  2.  4|  polymerase chain reaction, Human Mutation, 16 (1): 77 – 85.~ ~Rothman