Category:Genetics stubs
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Pages in category "Genetics stubs"
The following 200 pages are in this category, out of 1,373 total.
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A
- ABCC3
- Abo blood type
- Acanthocytosis chorea
- Accessory chromosome
- Acentric chromosome
- Acentric fragment
- Acid maltase
- Acrocentric chromosome
- Activator (genetics)
- ADD1
- ADD2
- Additive genetic effects
- Adenomatous polyposis coli
- Adenylosuccinate lyase deficiency
- Adjacent segregation
- Admixture mapping
- Advanced paternal age
- Affine
- Agar gel electrophoresis
- Agnatic
- Allele
- Allele frequency
- Allele-specific oligonucleotide
- Allelic heterogeneity
- Allopolyploid
- Allosome
- Alpha globin
- Alpha thalassemia trait
- Alternative flatworm mitochondrial code
- Alternative splicing
- Alternative yeast nuclear code
- Alu
- Alu element
- Alu family
- Amaurosis congenita of Leber
- Amaurotic familial idiocy
- Amber codon
- Amber mutation
- Amber suppressor
- Amelanism
- Ames test
- Amino acid substitution
- Amorphic mutation
- Amphidiploid
- Ancestors
- Androgenesis
- Animal genetics
- Aniridia type 2
- Anlage
- Anterior segment mesenchymal dysgenesis
- Antihemophilic factor
- Antisense drug
- Antisense strand
- Antitermination
- Apadamtase alfa
- Apolipoprotein b deficiency
- Aristaless related homeobox
- ARL13B
- Artificial selection
- Arylsulfatase B
- Ascidian mitochondrial code
- Ashbya gossypii
- Atacama skeleton
- Athymic mouse
- ATM serine/threonine kinase
- ATP5F1A
- Autarchic
- Autism Genetic Resource Exchange
- Auto-segregation
- Autoimmune regulator
- Autosomal chromosome
- Autosomal dominant
- Autosomal dominant disorders
- Autosomal inheritance
- Autosomal recessive disorders
- Autosome
B
- B chromosome
- B chromosomes
- Back mutation
- Backcrossing
- Baco 1
- Bacterial genetics
- Bacterial, archaeal and plant plastid code
- Balanced polymorphism
- Balding–Nichols model
- BARHL2
- Base analogue
- Base pairing
- Base sequence
- Base sequence analysis
- Base-pair substitution
- Basic helix-loop-helix leucine zipper transcription factors
- BBX (gene)
- Behavior Genetics Association
- Behavioural genetics
- Benign familial infantile epilepsy
- BHLHA9
- Bicoid 3′-UTR regulatory element
- Bietti's crystalline dystrophy
- Biochemical genetics
- Biological determinism
- Biotype
- Biparental inheritance
- Bivalent chromosome
- Blastocrithidia nuclear code
- Blending theory
- Blepharisma nuclear code
- Blood line
- Blue cone monochromatism
- Blue sclera
- Boveri–Sutton chromosome theory
- Brachydactyly hypertension
- Branch migration
- Branchial arch syndrome X linked
- Breakage-fusion-bridge cycle
- Breast cancer–related regulator of tp53
- Bronze diabetes
- Bruton tyrosine kinase
- Bruton's tyrosine kinase
- Bubble boy disease
- Buntinx–Lormans–Martin syndrome
- Burn–Goodship syndrome
C
- C-myc Internal Ribosome Entry Site (IRES)
- C10orf67
- C11orf1
- C11orf16
- C14orf119
- C16orf46
- CAAT box
- CADASIL syndrome
- Cafe au lait spot
- Café au lait spot
- CALCRL
- Calderon–Gonzalez–Cantu syndrome
- Calico cat
- Cancer genome sequencing
- Candidate gene
- Candidate Gene
- Carnosinase deficiency
- Cas9
- Cat body-type mutation
- Cat coat genetics
- Cav2.1
- CDKL5 deficiency disorder
- Cecato De lima Pinheiro syndrome
- Cell Cycle
- Cell cycle checkpoint
- Centromere
- CEP290
- CHD7
- Chi sequence
- Chi site
- Christmas disease
- Chromatin remodeling
- Chromatin remodelling
- Chromatin structure
- Chromo shadow domain
- Chromosomal aberration
- Chromosomal abnormality
- Chromosomal crossover
- Chromosomal deletion
- Chromosomal duplication
- Chromosomal inversion
- Chromosomal mutation
- Chromosomal polymorphism
- Chromosomal rearrangement
- Chromosomal satellite
- Chromosomal sex
- Chromosomal translocation
- Chromosomal translocations
- Chromosome 1
- Chromosome 1 ring
- Chromosome 1, deletion q21 q25
- Chromosome 1, duplication 1p21 p32
- Chromosome 1, monosomy 1p22 p13
- Chromosome 1, monosomy 1p31 p22
- Chromosome 1, monosomy 1p32
- Chromosome 1, monosomy 1p34 p32
- Chromosome 1, monosomy 1q25 q32
- Chromosome 1, monosomy 1q32 q42
- Chromosome 1, monosomy 1q4
- Chromosome 1, q42 11 q42 12 duplication
- Chromosome 1, trisomy 1q32 qter
- Chromosome 1, trisomy 1q42 qter
- Chromosome 1, uniparental disomy 1q12 q21
- Chromosome 10 ring
- Chromosome 10, distal trisomy 10q
- Chromosome 10, monosomy 10q
- Chromosome 10, trisomy 10p
- Chromosome 10, trisomy 10pter p13
- Chromosome 10, trisomy 10q
- Chromosome 10, uniparental disomy of
- Chromosome 11, deletion 11p
- Chromosome 11, partial trisomy 11q
- Chromosome 11-14 translocation
