Genetic Dosage and Chromosome Abnormalities

Related lectures (32)

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

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

Explores mutations, phenotype effects, environmental influences, meiosis, genetic shuffling, and chromosomal abnormalities.

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

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

Explores the genetic mechanisms of Prader Willi syndrome and DNA analysis techniques.

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

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

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

Explores DNA fundamentals, structure, production, and engineering of DNA-based materials, including hydrogels and particles.