Category:Genetics stubs
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Subcategories
This category has the following 4 subcategories, out of 4 total.
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- Genetic disorder stubs (254 P)
- Genetics journal stubs (62 P)
Pages in category "Genetics stubs"
The following 200 pages are in this category, out of approximately 545 total. This list may not reflect recent changes.
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- A-site
- ACE model
- Active chromatin sequence
- Adam's Curse
- Adapter (genetics)
- Additive genetic effects
- ADE model
- Allelic heterogeneity
- Alternative flatworm mitochondrial code
- Alternative yeast nuclear code
- Ambidirectional dominance
- American Society of Gene and Cell Therapy
- Animal Genome Size Database
- Arginine catabolic mobile element
- Artificially Expanded Genetic Information System
- Ascidian mitochondrial code
- Atypical SLCs
B
C
- Cer6 (retrotransposon)
- Chimera (molecular biology)
- Chimeraplasty
- Chordate genomics
- Choriogenesis
- Chromosome jumping
- Chromosome landing
- Chromosome regions
- Ciliate, dasycladacean and hexamita nuclear code
- Cis-acting replication element
- Cistrome
- Cistron
- Clinical Genome Resource
- Codon reassignment
- Coenogamete
- Cohorts for Heart and Aging Research in Genomic Epidemiology
- Collagen, type VI, alpha 5
- Collagen, type XX, alpha 1
- Collagen, type XXI, alpha 1
- Collagen, type XXII, alpha 1
- Collagen, type XXVIII, alpha 1
- Combined Annotation Dependent Depletion
- Composite transposon
- Concatemer
- Congenic
- Constitutive ablation
- Cooperative Human Linkage Center
- Core binding factor
- Cot filtration
- CPS operon
- Crossover value
- Cryptic relatedness
- Cryptogene
- CYP6 family
- CYP9 family
- CYP10 family
- CYP11 family
- CYP11A2
- CYP12 family
- CYP13 family
- CYP14 family
- CYP15 family
- CYP16 family
- CYP18 family
- CYP23 family
- CYP25 family
- CYP26 family
- CYP27 family
- CYP52 family
- CYP53 family
- CYP55 family
- CYP74 family
- CYP76 family
- CYP105 family
- CYP107 family
- CYP109 family
- CYP123 family
- CYP139 family
- CYP147 family
- CYP197 family
- CYP305 family
- CYP710 family
- Cytogenetic notation
- Cytonuclear discordance
D
- D arm
- De Finetti diagram
- De novo mutation
- DEL17P13.1
- Deletion mapping
- Derivative chromosome
- Desoxyribonucleate
- Direct repeat
- DNA analyzer
- DNA Day
- DNA ligase (NAD+)
- DNA machine
- DNA Repair and Mutagenesis
- DNA-templated organic synthesis
- Duke University Institute for Genome Sciences and Policy
- Dyad symmetry
- Dynamic mutation
E
- E-site
- Echinoderm and flatworm mitochondrial code
- Ecological Genetics (book)
- Ecotypic variation
- Effective number of codons
- EHA101
- Electroelution
- Electronic Medical Records and Genomics Network
- Electropherogram
- Elston–Stewart algorithm
- EMX homeogene
- Encyclopedia of Genetics
- Enterosoma genetic code
- Estonian Biocentre
- European Society of Gene and Cell Therapy
- European Society of Human Genetics
- Exploding the Gene Myth
- Expression cloning
- Expressome
- External transcribed spacer
- Extrachromosomal array
G
- Gag/pol translational readthrough site
- Gendicine
- Gene orders
- Gene pyramiding
- Gene stacking
- Gene therapy for blood diseases
- GeneReviews
- GeneSweep
- The Genetic Basis of Evolutionary Change
- Genetic demixing
- Genetic Information Research Institute
- Genetic structure
- Geneticization
- Genome in a Bottle
- Genome India Project
- Genome-wide significance
- Genomic DNA
- Genomic signature
- Genoscope
- Genosome
- GIANT consortium
- Glycol nucleic acid
- GRAFS
- Gruber Prize in Genetics
H
- Haldane's sieve
- Haplogroup A-P305
- Haplogroup C-B477
- Haplogroup C-V20
- Haplogroup CZ
- Haplogroup D-Z27276
- Haplogroup JT
- Haplogroup L4
- Haplogroup L5
- Haplogroup L6
- Haplogroup P (mtDNA)
- Haplogroup pre-JT
- Haplogroup S (mtDNA)
- Haplotype 35
- Haplotype block
- Haseman–Elston regression
- HCT116 cells
- Hexadimethrine bromide
- High-mobility group
- HLA-B22
- HLA-Cw4
- HMGA
- Hologenomics
- Homogeneously staining region
- Homothorax
- Horizontal resistance
- HT-TALENS
- Human Epigenome Project
- Human Genetics Society of Australasia
- Human identical sequence
- Human satellite II
- Humster
- Hybrid growth disorders