Lectures related to Monozygotic Twins: DNA Profile and Paternity Test

DNA Technology: PCR and Genetic Diversity

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

Genetic Dosage and Chromosome Abnormalities

Explores genetic dosage, X chromosome inactivation, and chromosome abnormalities, illustrated by real-life examples and genetic concepts.

DNA Analysis: Trisomy Detection and Paternity Testing

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

Genetic Dosage and Chromosome 21

Explores genetic dosage, Chromosome 21, X-inactivation, and X-linked inheritance.

Chromosome Anomalies: Trisomy and Uniparental Disomy

Covers DNA replication, PCR technology, microsatellites, placental trisomy, and genetic anomalies in prenatal testing.

DNA Profiling: PCR and Genetic Markers

Explains PCR, microsatellite analysis, DNA profiling in forensics, and legal requirements.

Cellular Biology: Mitosis and Meiosis Overview

Covers cellular biology, focusing on mitosis, meiosis, and the cell cycle processes.

Genetics: History and Key Concepts

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

Patterns of Inheritance in Biology

Explores major themes in biology, patterns of inheritance, Mendel's laws, genetic defects, and the impact of the environment on phenotype.

Genetic Transmission: Probability and Disease

Explores genetic transmission and disease inheritance probabilities, emphasizing real-life applications and complex genetic scenarios.

Chromosome Variation

Explores variations in chromosome numbers and structure, including deletions, duplications, inversions, and translocations.

Placental Trisomy 7: Uniparental Disomy and Genetic Testing

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

Meiosis: Chromosome Division and Genetic Shuffling

Explores meiosis, focusing on chromosome division, genetic shuffling, and consequences of errors.

Chromosomal Dosage and Genetic Disorders

Explores chromosomal dosage, genetic disorders, inheritance patterns, and X chromosome inactivation.

Genomic Medicine: Ethics and Applications

Explores genomic medicine, covering genetic determinism, personalized medicine, genetic anomalies, and ethical considerations.

Genetic Inheritance: Chromosomes and Probabilities

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

Post-Genomics and Health Challenges

By Dr. Luca Chiapperino delves into the implications of post-genomics on health and society, focusing on the molecularization of our biography, experiences, and living environment.

Genomic Medicine: Personalized Health

Delves into genomic medicine, emphasizing personalized health and genetic factors associated with disease.

Genomics: Transposable Elements and DNA Fingerprinting

Explores transposable elements in the genome and the use of microsatellites for DNA fingerprinting.

Genetic Disorders: Chromosomal Aberrations

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