Chromosome Anomalies: Trisomy and Uniparental Disomy

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Delves into the molecular basis of genetic diseases, discussing specific examples like Phenylketonuria and Haemophilia A, and the development of small molecule drugs for genetic disorders.

DNA Technology: PCR and Genetic Diversity

Explores DNA technology through PCR, genetic diversity, forensic applications, and genetic disorders.

Genetic Disorders: Chromosomal Aberrations

Explores sex determination, chromosomal aberrations, and genetic diseases, including deletions, duplications, and non-disjunction during meiosis.

Monozygotic Twins: DNA Profile and Paternity Test

Explores monozygotic twins' genetics, paternity testing with microsatellites, trisomy 21 detection, and pre-implantation diagnostics.

Placental Trisomy 7: Uniparental Disomy and Genetic Testing

Explores a case of placental trisomy 7 and its implications on genetic testing.

Genetics: History and Key Concepts

Covers the history of genetics, key concepts, DNA structure, gene expression, and genetic engineering.

DNA Analysis: Trisomy Detection and Paternity Testing

Explores DNA analysis for trisomy detection and paternity testing using microsatellites and probabilistic calculations.

Genetic Inheritance: Chromosomes and Probabilities

Explores Mendelian genetics, covering chromosomal theory, genetic ratios, Chi-square analysis, and human trait pedigrees.

DNA Replication: Mechanisms and Applications

Explores DNA replication, the genetic code, PCR applications, and forensic testing.

Genetic Mutations: Causes and Effects

Explores genetic mutations, chromosomal abnormalities, DNA repair, and disease implications.