General Genetics Concepts
- adenine
- adenosine deaminase deficiency (ADA)
- adenovirus
- Alagille syndrome
- allele
- amino acids
- animal model
- antibody
- antisense
- apoptosis
- ataxia-telangiectasia
- Autoimmune Lymphoproliferative syndrome (ALPS)
- autosomal dominant
- autosome
- bacteria
- bacterial artificial chromosome (BAC)
- base pair
- birth defect
- bone marrow transplantation
- BRCA1/BRCA2
- cancer
- candidate gene
- carcinoma
- carrier
- cDNA library
- cell
- centimorgan
- centromere
- chromosome
- Chromosomal translocation
- cloning
- codon
- Congenital disorder
- contig
- craniosynostosis
- cystic fibrosis
- cytogenetic map
- cytosine
- deletion
- deoxyribonucleic acid (DNA)
- diabetes mellitus
- diploid
- DNA replication
- DNA sequencing
- dominant
- double helix
- duplication
- electrophoresis
- Ellisvan Creveld syndrome
- enzyme
- exon
- familial Mediterranean fever
- fibroblasts
- fluorescence in situ hybridization (FISH)
- Fragile X syndrome
- gene
- gene amplification
- gene expression
- gene library
- gene mapping
- gene pool
- gene therapy
- gene transfer
- genetic code
- ATGC
- genetic counseling
- genetic linkage
- genetic map
- genetic marker
- genetic screening
- genome
- genotype
- germ line
- guanine
- haploid
- haploinsufficiency
- hematopoietic stem cell
- hemophilia
- heterozygous
- highly conserved sequence
- Hirschsprung's disease
- holoprosencephaly
- homologous recombination
- homozygous
- human artificial chromosome (HAC)
- Human Genome Project
- human immunodeficiency virus (HIV)
- acquired immunodeficiency syndrome (AIDS)
- Huntington's disease
- hybridization
- immunotherapy
- in situ hybridization
- inherited
- insertion
- intellectual property rights
- intron
- Jurassic Park (genetics of)
- karyotype
- knockout
- leukemia
- locus
- LOD score
- lymphocyte
- malformation
- Gene mapping
- marker
- melanoma
- Mendel, Johann (Gregor)
- Mendelian inheritance
- messenger RNA
- mRNA
- metaphase
- microarray technology
- microsatellite
- mitochondrial DNA
- monosomy
- mouse model
- multiple endocrine neoplasia, type 1
- MEN1)
- mutation
- neurofibromatosis
- Niemann-Pick disease, type C (NPC)
- non-coding DNA
- non-directiveness
- nonsense mutation
- Northern blot
- nucleotide
- nucleus
- oligo
- oncogene
- oncovirus
- p53
- Parkinson's disease
- Particulate inheritance theory
- patent
- pedigree
- peptide
- phenotype
- physical map
- polydactyly
- polymerase chain reaction (PCR)
- polymorphism
- positional cloning
- primary immunodeficiency
- primer
- probe
- promoter
- pronucleus
- prostate cancer
- protease
- protein
- pseudogene
- recessive
- recombinant DNA
- repressor
- restriction enzymes
- restriction fragment length polymorphism (RFLP)
- retrovirus
- ribonucleic acid (RNA)
- ribosome
- risk communication
- sequence-tagged site (STS)
- severe combined immunodeficiency (SCID)
- sex chromosome
- sex-linked
- shotgun sequencing
- sickle cell disease
- single-nucleotide polymorphisms (SNPs)
- somatic cells
- Southern blot
- spectral karyotype (SKY)
- substitution
- suicide gene
- syndrome
- technology transfer
- thymine
- transgenic
- trisomy
- tumor suppressor gene
- uracil
- vector
- Western blot
- Wolfram syndrome
- yeast artificial chromosome (YAC)
Read more about this topic: Outline Of Genetics
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