Chromosomal Dosage and Genetic Disorders

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Related lectures (32)

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Prader-Villy Syndrome: Genetic Mechanisms and Clinical Implications

Explores the genetic basis of Prader-Villy syndrome and its comparison with Angelman syndrome, emphasizing DNA methylation patterns and chromosomal abnormalities.

Genetic Distance Calculation

Explores genetic distance calculation, sequence alignment, and the impact of friction.

Genetic Disorders and Hemoglobin Structure

Explores genetic disorders, hemoglobin structure, sickled cells, and electrophoresis techniques.

Chromosome Variation

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

Meiosis: Chromosome Division and Genetic Shuffling

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

Genetics: Chromosome Inheritance

Covers the basics of genetics, inheritance of alleles, genotype-phenotype relationship, and population genetics.

Chromosome Anomalies: Trisomy and Uniparental Disomy

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

Sex Determination

Explores sex determination mechanisms in reptiles, humans, and anomalies like Klinefelter and Turner syndromes, as well as the sex ratio.

Evolution of Sex Chromosomes

Explores the evolution of sex chromosomes, the shrinking of the Y chromosome, and Langer mesomelic dysplasia.

Chromosomes and Meiosis: Understanding Genetic Variation

Explains chromosome duplication, separation, meiosis stages, and genetic variation consequences.