Category:Genetics stubs
From WikiMD's Wellness Encyclopedia
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Subcategories
This category has the following 2 subcategories, out of 2 total.
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Pages in category "Genetics stubs"
The following 200 pages are in this category, out of 1,317 total.
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- 17q21.31 microdeletion syndrome
- 22q11.2 distal deletion syndrome
- 3' end
- 40S ribosomal protein S11
- 40S ribosomal protein S24
- 40S ribosomal protein S28
- 47, XYY syndrome
- 5' untranslated regions
- 5′ flanking region
- 60S ribosomal protein L35a
- ABCC3
- Abl gene
- Accessory chromosome
- Acentric chromosome
- Acentric fragment
- Acid maltase
- Acrocentric chromosome
- ACTG1
- Activator (genetics)
- Additive genetic effects
- Adenomatous polyposis coli
- Adenylosuccinate lyase deficiency
- ADH1B
- Adjacent segregation
- Admixture mapping
- Advanced paternal age
- Agar gel electrophoresis
- Agnatic
- Allele
- Allele frequency
- Allele-specific oligonucleotide
- Allelic heterogeneity
- Allopolyploid
- Allosome
- Allozyme
- Alpha globin
- Alpha thalassemia trait
- Alternative splicing
- Alu
- Alu element
- ALX1
- ALX4
- Amaurosis congenita of Leber
- Amaurotic familial idiocy
- Amber codon
- Amber mutation
- Amber suppressor
- Amelanism
- Ames test
- Ames Test
- Amphidiploid
- Ancestors
- Androgenesis
- Aneuploidy
- Animal genetics
- Anterior segment mesenchymal dysgenesis
- Antihemophilic factor
- Antisense drug
- Antisense strand
- Antitermination
- Apadamtase alfa
- APC gene
- ARHGEF9
- Aristaless related homeobox
- ARL13B
- Artificial selection
- Arylsulfatase B
- ASXL3
- Atacama skeleton
- Athymic mouse
- ATM serine/threonine kinase
- ATP5F1A
- ATXN2
- Autarchic
- Autism Genetic Resource Exchange
- Auto-segregation
- Autoimmune regulator
- Autosomal
- Autosomal chromosome
- Autosomal dominant
- Autosomal dominant disorders
- Autosomal recessive disorders
- Autosome
- Axial Biotech
- B chromosome
- B chromosomes
- Back mutation
- Backcrossing
- Bacterial genetics
- Balanced polymorphism
- Balding–Nichols model
- BARHL2
- Base analogue
- Base pairing
- Base sequence
- Base sequence analysis
- Basic helix-loop-helix leucine zipper transcription factors
- BBX (gene)
- BCKDHA
- 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
- Blood line
- Blue cone monochromatism
- Blue sclera
- Boveri–Sutton chromosome theory
- Branch migration
- BRCA mutation
- Breakage-fusion-bridge cycle
- Bronze diabetes
- Bruton tyrosine kinase
- Bruton's tyrosine kinase
- Bubble boy disease
- Buccal swab
- C14orf119
- CAAT box
- CADASIL syndrome
- Cafe au lait spot
- Café au lait spot
- CALCRL
- Calderon–Gonzalez–Cantu syndrome
- Calico cat
- Camptodactyly, tall stature, and hearing loss syndrome
- Cancer genome sequencing
- Cancer syndrome
- Candidate gene
- Candidate Gene
- Carnosinase deficiency
- Cas9
- Cat body-type mutation
- Cat coat genetics
- Cav2.1
- CCDC177
- CCM2
- CDAN1
- CDKL5 deficiency disorder
- CDNA
- Cecato De lima Pinheiro syndrome
- Cell Cycle
- Cell cycle checkpoint
- Centromere
- CEP290
- Ceroid lipofuscinois, neuronal 6, late infantile
- CHD7
- Chi sequence
- Chi site
- Chimera (genetics)
- Chondrodysplasia, Grebe type
- Christmas disease
- Chromatin remodeling
- Chromatin remodelling
- Chromatin structure
- Chromo shadow domain
- Chromosomal aberration
- Chromosomal abnormality
- Chromosomal crossover
- Chromosomal deletion
- Chromosomal duplication
- Chromosomal inversion
- Chromosomal microarray analysis
- Chromosomal mutation
- Chromosomal polymorphism
- Chromosomal rearrangement
- Chromosomal sex
- Chromosomal translocation
- Chromosomal translocations
- Chromosome 1 ring
- Chromosome 1, deletion q21 q25
- 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, trisomy 1q32 qter
- Chromosome 1, trisomy 1q42 qter
- Chromosome 1, uniparental disomy 1q12 q21
- Chromosome 10 ring
- Chromosome 10, monosomy 10q
- Chromosome 10, trisomy 10p
- Chromosome 10, trisomy 10q
- Chromosome 11 (human)
- Chromosome 11, deletion 11p
- Chromosome 11-14 translocation
- Chromosome 11p, partial deletion
- Chromosome 11q partial deletion
- Chromosome 11q trisomy
- Chromosome 12
- Chromosome 12 (human)
- Chromosome 12 ring
- Chromosome 12, 12p trisomy
