Polymorphism

A genetic characteristic with more than one common form in a population.

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Teaching Genetics

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  • Cytogenetics

  • De novo mutation

  • Degree of relationship

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  • DNA

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  • Dysmorphic

  • Empiric risk

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  • First-degree relative

  • FISH: fluorescence in situ hybridisation

  • Gamete

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  • Gene deletion(s)

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  • Genetic heterogeneity

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  • Genetics

  • Genome

  • Genome-wide Association Study (GWAS)

  • Genomic medicine

  • Genotype

  • Gonadal/germline mosaicism

  • GWAS

  • Heterozygote (Heterozygous): Carrier

  • Homologous

  • Homozygote (Homozygous)

  • Incidence

  • Inheritance

  • Karyotype

  • Liability

  • Linkage analysis

  • Locus (loci)

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  • Mendelian inheritance

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  • Mitochondrial condition

  • Mitochondrial inheritance

  • Monosomy (Monosomic)

  • Mosaicism (mosaic)

  • Multifactorial inheritance

  • Mutation

  • New mutation

  • Offspring risk

  • Patterns of inheritance

  • Pedigree diagram

  • Penetrance

  • Personalised medicine

  • Pharmacogenetics

  • Pharmacogenomics

  • Phenotype

  • Polymerase chain reaction (PCR)

  • Polymorphism

  • Premutation

  • Prenatal diagnosis

  • Presymptomatic testing

  • Prevalence

  • Recurrence risk

  • Second-degree relative

  • Sex chromosome

  • Sib/sibling

  • Single gene disorder

  • Somatic cell

  • Sporadic

  • Stratified medicine

  • Syndrome

  • Teratogen

  • Third-degree relative

  • Trait

  • Transcription

  • Translation

  • Translocation

  • Trinucleotide (triplet) repeat

  • Trisomy (Trisomic)

  • X-Chromosome inactivation

  • X-linked dominant

  • X-linked recessive