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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 cloning codon congenital contig craniosynostosis cystic fibrosis cytogenetic map cytosine
deletion deoxyribonucleic acid (DNA) diabetes mellitus diploid DNA replication DNA sequencing dominant double helix duplication electrophoresis Ellis - van Creveld syndrome enzyme exon familial Mediterranean fever fibroblasts fluorescence in situ hybridization (FISH) Fragile X syndrome gene gene amplification gene expression gene mapping gene pool gene therapy gene transfer genetic code (ATGC) genetic counseling 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 karyotype knockout leukemia library linkage locus LOD score lymphocyte malformation 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 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 translocation trisomy tumor suppressor gene uracil vector Western blot Wolfram syndrome yeast artificial chromosome (YAC)
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