Chromosome Anomalies: Trisomy and Uniparental Disomy

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

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.

Chromosome 7: Trisomy Correction Mechanisms

Explores trisomy correction mechanisms, mosaicism, and genetic disorder diagnosis challenges.

Genetic Dosage and Chromosome Abnormalities

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

Chromosomal Dosage and Genetic Disorders

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

Meiosis: Chromosome Division and Genetic Shuffling

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

Cellular Biology: Mitosis and Meiosis Overview

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

Mutations and Genetic Variability

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

Genetic Dosage and Chromosome 21

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

Chromosome Variation

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