Category:Genetics stubs
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Pages in category "Genetics stubs"
The following 200 pages are in this category, out of 842 total.
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- 13q deletion syndrome
- 1p36 deletion syndrome
- 1q21.1 duplication syndrome
- 22q11.2 distal deletion syndrome
- 22q13 deletion syndrome
- 2p15-16.1 microdeletion syndrome
- 2q37 deletion syndrome
- 2q37 monosomy
- 3-Hydroxyisobutyryl-CoA deacylase deficiency
- 3C syndrome
- 3q29 microdeletion syndrome
- 40S ribosomal protein S11
- 40S ribosomal protein S24
- 40S ribosomal protein S28
- 47, XYY syndrome
- 6-phosphogluconate dehydrogenase deficiency
- 6-Pyruvoyltetrahydropterin synthase deficiency
- 60S ribosomal protein L35a
- 8p23.1 duplication syndrome
- ABCC3
- Acentric fragment
- ADH1B
- Agnatic
- Allele
- Allele frequency
- Allelic heterogeneity
- Alternative splicing
- Alu
- Alu element
- ALX1
- ALX4
- Ames test
- Androgenesis
- Aneuploidy
- Anterior segment mesenchymal dysgenesis
- Antitermination
- Apadamtase alfa
- ARHGEF9
- Aristaless related homeobox
- ARL13B
- Arylsulfatase B
- ASXL3
- ATM serine/threonine kinase
- ATP5F1A
- Autarchic
- Autism Genetic Resource Exchange
- Autoimmune regulator
- Autosomal dominant
- Autosomal recessive disorders
- Autosome
- Axial Biotech
- B chromosome
- Back mutation
- Backcrossing
- Bacterial genetics
- Balding–Nichols model
- BARHL2
- 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
- Biological determinism
- Biotype
- Biparental inheritance
- Blood line
- Boveri–Sutton chromosome theory
- BRCA mutation
- Bruton's tyrosine kinase
- Buccal swab
- CALCRL
- Calico cat
- Camptodactyly, tall stature, and hearing loss syndrome
- Cancer genome sequencing
- Candidate gene
- Cas9
- Cav2.1
- CCDC177
- CCM2
- CDAN1
- CDKL5 deficiency disorder
- Cecato De lima Pinheiro syndrome
- Cell Cycle
- Cell cycle checkpoint
- Centromere
- CEP290
- CHD7
- Chi site
- Chimera (genetics)
- Chondrodysplasia, Grebe type
- Chromatin remodeling
- Chromosomal crossover
- Chromosomal inversion
- Chromosomal rearrangement
- Chromosomal translocation
- 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 11-14 translocation
- Chromosome 11q trisomy
- Chromosome 12
- Chromosome 12 ring
- Chromosome 12, 12p trisomy
- Chromosome 12, trisomy 12q
- Chromosome 12p deletion
- Chromosome 13
- Chromosome 13 duplication
- Chromosome 13 ring
- Chromosome 13p duplication
- Chromosome 13q trisomy
- Chromosome 13q-mosaicism
- Chromosome 14 trisomy
- Chromosome 14, trisomy mosaic
- Chromosome 15q, tetrasomy
- Chromosome 16
- Chromosome 17
- Chromosome 17 deletion
- Chromosome 17 ring
- Chromosome 17, trisomy 17p
- Chromosome 17, trisomy 17q22
- Chromosome 18, deletion 18q23
- Chromosome 19
- Chromosome 19 ring
- Chromosome 19, trisomy 19q
- Chromosome 2, monosomy 2p22
- Chromosome 2, monosomy 2q24
- Chromosome 2, trisomy 2p
- Chromosome 2, Trisomy 2p13 p21
- Chromosome 2, trisomy 2pter p24
- Chromosome 2, trisomy 2q
- Chromosome 20, deletion 20p
- Chromosome 20, duplication 20p
- Chromosome 20, trisomy
- Chromosome 21 ring
- Chromosome 21, tetrasomy 21q
- Chromosome 22, monosome mosaic
- Chromosome 22, trisomy q11 q13
- Chromosome 3
- Chromosome 3, monosomy 3p14 p11
- Chromosome 3, monosomy 3p2
- Chromosome 3, monosomy 3p25
- Chromosome 3, monosomy 3q13
- Chromosome 3, monosomy 3q21 23
- Chromosome 3, monosomy 3q27
- Chromosome 3, trisomy 3p
- Chromosome 3, trisomy 3p25
- Chromosome 3, trisomy 3q
- Chromosome 3, trisomy 3q13 2 q25
- Chromosome 3, Trisomy 3q2
- Chromosome 4 ring
- Chromosome 4, monosomy 4p14 p16
- Chromosome 4, monosomy 4q
- Chromosome 4, monosomy 4q32
- Chromosome 4, Trisomy 4p
- Chromosome 4, trisomy 4q
- Chromosome 4, trisomy 4q21
- Chromosome 5, monosomy 5q35
- Chromosome 5, trisomy 5p
- Chromosome 5, trisomy 5q
- Chromosome 6
- Chromosome 6 ring
- Chromosome 6, deletion 6q13 q15
- Chromosome 6, monosomy 6q
- Chromosome 6, trisomy 6p
- Chromosome 6, trisomy 6q
- Chromosome 7
- Chromosome 7 ring
- Chromosome 7, monosomy
- Chromosome 7, monosomy 7q21
- Chromosome 7, monosomy 7q3
- Chromosome 7, trisomy 7p
- Chromosome 7, trisomy 7p13 p12 2
- Chromosome 7, trisomy 7q
- Chromosome 8
- Chromosome 8 deletion
- Chromosome 8 ring
- Chromosome 8, monosomy 8p
- Chromosome 8, monosomy 8p2
- Chromosome 8, monosomy 8p23 1
- Chromosome 8, monosomy 8q
- Chromosome 9
- Chromosome 9 Ring
- Chromosome 9, duplication 9q21
- Chromosome instability
