Category:Genetics stubs
From WikiMD's Wellness Encyclopedia
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Pages in category "Genetics stubs"
The following 200 pages are in this category, out of 1,577 total.
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- 17q21.31 microdeletion syndrome
- 22q11.2
- 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
- Abo blood type
- Acanthocytosis chorea
- Accessory chromosome
- Acentric chromosome
- Acentric fragment
- Acid maltase
- Acrocentric chromosome
- ACTG1
- Activator (genetics)
- ADD1
- ADD2
- 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
- Alstrom
- Alternative flatworm mitochondrial code
- Alternative splicing
- Alternative yeast nuclear code
- Alu
- Alu element
- Alu family
- Alu sequence
- ALX1
- ALX4
- Amaurosis congenita of Leber
- Amaurotic familial idiocy
- Amber codon
- Amber mutation
- Amber suppressor
- Amelanism
- Ames test
- Ames Test
- Amino acid substitution
- AMMECR1
- Amorphic mutation
- AMPD2
- Amphidiploid
- Ancestors
- Androgenesis
- Aneuploidy
- Animal genetics
- Aniridia type 2
- Anterior segment mesenchymal dysgenesis
- Antihemophilic factor
- Antisense drug
- Antisense strand
- Antitermination
- Apadamtase alfa
- APC gene
- Apolipoprotein b deficiency
- ARHGEF9
- Aristaless related homeobox
- ARL13B
- Artificial selection
- Arylsulfatase B
- Ascidian mitochondrial code
- Ashbya gossypii
- ASXL1
- 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 inheritance
- Autosomal recessive disorders
- Autosome
- Axial Biotech
- 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)
- 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
- 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
- BRCA mutation
- Breakage-fusion-bridge cycle
- Breast cancer–related regulator of tp53
- Bronze diabetes
- Bruton tyrosine kinase
- Bruton's tyrosine kinase
- Bubble boy disease
- Buccal swab
- C10orf67
- C11orf16
- C12orf40
- C14orf119
- C16orf46
- 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
- CBX2
- CCDC177
- CCM2
- CDAN1
- CDKL5 deficiency disorder
- CDNA
- Cecato De lima Pinheiro syndrome
- Cell Cycle
- Cell cycle checkpoint
- CENPC1
- Centromere
- CEP104
- CEP120
- CEP128
- CEP152
- CEP290
- CEP70
- CEP78
- Ceroid lipofuscinois, neuronal 6, late infantile
- CG100649
- CHARGE study
- CHD1L
- CHD2
- CHD4
- CHD7
- Chi sequence
- Chi site
