| Lecture 1 |
lecture 1 introduction to genetics chapter 1 |
| Lecture 1 |
lecture 2 Autosomal dominant inheritance chapter 1 |
| Lecture 1 |
lecture 3 autosomal recessive inheritance chapter 1 |
| Lecture 1 |
lecture 4 x linked recessive inheritance chapter 1 |
| Lecture 1 |
lecture 5 x linked dominant inheritance chapter 1 |
| Lecture 2 |
lecture 5 x linked dominant inheritance chapter 1 |
| Lecture 1 |
lecture 6 Mitochondrial inheritance chapter 1 |
| Lecture 2 |
lecture 6 Mitochondrial inheritance chapter 1 |
| Lecture 1 |
lecture 7 variable expression(Chapter 2) |
| Lecture 1 |
lecture 8 incomplete penetrance Chapter 2 |
| Lecture 1 |
lecture 9 trinucleotide repeat disorders disorders Chapter 2 |
| Lecture 1 |
lecture 10 imprinting Chapter 2 |
| Lecture 1 |
lecture 11karyotype and chromosome Chapter 3 |
| Lecture 1 |
lecture 12 chromosomal trisomies Chapter 3 |
| Lecture 1 |
lecture 13 sex chromosome disorder (Chapter 3) |
| Lecture 1 |
lecture 14 Down syndrome Chapter 3 |
| Lecture 1 |
lecture 15 hardy-weinberg equation chapter 4 |
| Lecture 2 |
Lecture 15 reciprocal translocation Chapter 3 |
| Lecture 1 |
lecture 16 application of HWE chapter 4 |
| Lecture 1 |
lecture 17 Fluorescence in situ Hybridization (FISH) Chapter 3 |
| Lecture 1 |
Lecture 18 Spectral Karyotyping chapter 3 |
| Lecture 2 |
Lecture 18 Spectral Karyotyping chapter 3 |
| Lecture 1 |
lecture 19 hardy-weinberg equation chapter 4 |
| Lecture 1 |
lecture 20 application of HWE chapter 4 |
| Lecture 1 |
lecture 21 Genetic variations chapter 4 |
