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