Pages that link to "Autosome"
← Autosome
Showing 50 items.
- American Quarter Horse (links | edit)
- Chromosome (links | edit)
- Clitoridectomy (links | edit)
- Chromatin (links | edit)
- Centromere (links | edit)
- DNA (transclusion) (links | edit)
- Down syndrome (links | edit)
- Genetics (links | edit)
- Genome (links | edit)
- Genetic disorder (links | edit)
- Genotype (links | edit)
- Haemophilia (links | edit)
- Histone (links | edit)
- Meiosis (links | edit)
- Mutation (links | edit)
- Maasai people (links | edit)
- Native Americans in the United States (links | edit)
- Nucleosome (links | edit)
- Ploidy (links | edit)
- Proto-Indo-Europeans (links | edit)
- Slavs (links | edit)
- Vedda (links | edit)
- XYY syndrome (links | edit)
- Trisomy (links | edit)
- Human genome (links | edit)
- East Slavs (links | edit)
- Turkic peoples (links | edit)
- Turner syndrome (links | edit)
- Sex-determination system (links | edit)
- Fragile X syndrome (links | edit)
- Euchromatin (links | edit)
- Heterochromatin (links | edit)
- Telomere (links | edit)
- Prader–Willi syndrome (links | edit)
- Canavan disease (links | edit)
- Caenorhabditis elegans (links | edit)
- Russians (links | edit)
- Serbs (links | edit)
- Polyploidy (links | edit)
- Selkirk Rex (links | edit)
- Nilotic peoples (links | edit)
- Dominance (genetics) (links | edit)
- Croats (links | edit)
- Maine Coon (links | edit)
- Roanoke Colony (links | edit)
- Mitochondrial DNA (links | edit)
- Brachydactyly (links | edit)
- Autosomal (redirect page) (links | edit)
- Ataxia (links | edit)
- American Quarter Horse (links | edit)
- Essential tremor (links | edit)
- Heredity (links | edit)
- Demographics of India (links | edit)
- Genomic imprinting (links | edit)
- Lafora disease (links | edit)
- Ploidy (links | edit)
- Demographics of Puerto Rico (links | edit)
- Absolute pitch (links | edit)
- Greeks (links | edit)
- Microsatellite (links | edit)
- Huntington's disease (links | edit)
- Sex-determination system (links | edit)
- Biology and sexual orientation (links | edit)
- Genomics (links | edit)
- List of genetic disorders (links | edit)
- Selkirk Rex (links | edit)
- Abetalipoproteinemia (links | edit)
- Akhal-Teke (links | edit)
- Appaloosa (links | edit)
- Scottish Fold (links | edit)
- Karyotype (links | edit)
- Corded Ware culture (links | edit)
- Warfarin (links | edit)
- Felis (links | edit)
- Deletion (genetics) (links | edit)
- Crossbill (links | edit)
- Keratoconus (links | edit)
- Arabian horse (links | edit)
- Gilbert's syndrome (links | edit)
- Székelys (links | edit)
- Night terror (links | edit)
- Fanconi anemia (links | edit)
- Lithuanians (links | edit)
- Gagauz people (links | edit)
- Gene duplication (links | edit)
- Propionic acidemia (links | edit)
- Chromosomal translocation (links | edit)
- Arginase (links | edit)
- Bedlington Terrier (links | edit)
- Ichthyosis (links | edit)
- Phenylthiocarbamide (links | edit)
- Insulin-like growth factor 1 (links | edit)
- Coefficient of relationship (links | edit)
- Portuguese Water Dog (links | edit)
- Online Mendelian Inheritance in Man (links | edit)
- Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency (links | edit)
- Irish people (links | edit)
- Laboratory mouse (links | edit)
- Glanzmann's thrombasthenia (links | edit)
- Hyperhidrosis (links | edit)
- Portuguese people (links | edit)
- White rhinoceros (links | edit)
- Persistent Müllerian duct syndrome (links | edit)
- Familial thoracic aortic aneurysm (links | edit)
- Alpha-mannosidosis (links | edit)
- Oculopharyngeal muscular dystrophy (links | edit)
- Robertsonian translocation (links | edit)
- Hurler syndrome (links | edit)
- Chorea-acanthocytosis (links | edit)
- Glomerulonephritis (links | edit)
- Keratosis pilaris (links | edit)
- Clitoromegaly (links | edit)
- Giant Schnauzer (links | edit)
- Chromosomal inversion (links | edit)
- Protein S deficiency (links | edit)
- Diastrophic dysplasia (links | edit)
- Cockayne syndrome (links | edit)
- Aldolase A (links | edit)
- Trimethylamine (links | edit)
- Mulibrey nanism (links | edit)
- Gerstmann–Sträussler–Scheinker syndrome (links | edit)
- Isovaleric acidemia (links | edit)
- Male reproductive system (links | edit)
- Leukodystrophy (links | edit)
- Meleda disease (links | edit)
- Y-STR (links | edit)
- Hartnup disease (links | edit)
- Giant axonal neuropathy (links | edit)
- Dysmetria (links | edit)
- Reciprocal cross (links | edit)
- Fraser syndrome (links | edit)
- Convict cichlid (links | edit)
- Locus (genetics) (links | edit)
- Polysomy (links | edit)
- List of organisms by chromosome count (links | edit)
- Abdallat–Davis–Farrage syndrome (links | edit)
- Sugarman syndrome (links | edit)
- Osteitis fibrosa cystica (links | edit)
- Crigler–Najjar syndrome (links | edit)
- Spasmodic torticollis (links | edit)
- Intraflagellar transport (links | edit)
- Mucolipidosis (links | edit)
- Chondrodystrophy (links | edit)
- Molecular anthropology (links | edit)
- Pantothenate kinase-associated neurodegeneration (links | edit)
- Hermansky–Pudlak syndrome (links | edit)
- Albright's hereditary osteodystrophy (links | edit)
- Glycogen branching enzyme (links | edit)
- Activated protein C resistance (links | edit)
- Salvador, Bahia (links | edit)
- Fountain syndrome (links | edit)
- Differential extraction (links | edit)
- XX male syndrome (links | edit)
- Pachyderma (links | edit)
- Celtic nations (links | edit)
- Short-chain acyl-coenzyme A dehydrogenase deficiency (links | edit)
- Kjer's optic neuropathy (links | edit)
- Zaspopathy (links | edit)
- Adenylosuccinate lyase deficiency (links | edit)
- Photic sneeze reflex (links | edit)
- Pseudoautosomal region (links | edit)
- ZW sex-determination system (links | edit)
- Centronuclear myopathy (links | edit)
- Dyschromatosis universalis hereditaria (links | edit)
- Congenital muscular dystrophy (links | edit)
- Pattern hair loss (links | edit)
- Reeler (links | edit)
- Gray-tailed vole (links | edit)
- Nezelof syndrome (links | edit)
- Phosphoglycerate kinase (links | edit)
- Mucolipidosis type IV (links | edit)
- Osteochondrodysplasia (links | edit)
- G banding (links | edit)
- Sitosterolemia (links | edit)
- Arylsulfatase A (links | edit)
- Budgerigar colour genetics (links | edit)
- Chromosome abnormality (links | edit)
- Apolipoprotein B deficiency (links | edit)
- Rhizomelic chondrodysplasia punctata (links | edit)
- Axenfeld–Rieger syndrome (links | edit)
- Kaufman oculocerebrofacial syndrome (links | edit)
- Dravet syndrome (links | edit)
- Derek Abbott (links | edit)
- Raine syndrome (links | edit)
- Mila Rechcigl (links | edit)
- Glutathione synthetase deficiency (links | edit)
- History of the Basques (links | edit)
- Laron syndrome (links | edit)
- Dermatopathia pigmentosa reticularis (links | edit)
- Hay–Wells syndrome (links | edit)
- Antithrombin III deficiency (links | edit)
- Pachyonychia congenita (links | edit)
- Derivative chromosome (links | edit)
- Currarino syndrome (links | edit)
- Somerton Man (links | edit)
- MNS antigen system (links | edit)
- 6-Phosphogluconate dehydrogenase (links | edit)
- Arterial tortuosity syndrome (links | edit)
- Zimmermann–Laband syndrome (links | edit)
- Zori–Stalker–Williams syndrome (links | edit)
- ACADSB (links | edit)
- Complement deficiency (links | edit)
- GLUT1 deficiency (links | edit)
- Drosophila hybrid sterility (links | edit)
- Hausa people (links | edit)
- Cystathioninuria (links | edit)
- 23andMe (links | edit)
- Scheie syndrome (links | edit)
- Bietti's crystalline dystrophy (links | edit)
- Chromosomal rearrangement (links | edit)
- Sex-limited genes (links | edit)
- Guanidinoacetate methyltransferase deficiency (links | edit)
- MOWA Band of Choctaw Indians (links | edit)
- Pelger–Huët anomaly (links | edit)
- White Mexicans (links | edit)
- Lavender foal syndrome (links | edit)
- MAP3K1 (links | edit)
- EXT2 (gene) (links | edit)
- NT5C3 (links | edit)
- Proteoglycan 4 (links | edit)
- CHKB (gene) (links | edit)
- Inosine-5′-monophosphate dehydrogenase (links | edit)
- Keutel syndrome (links | edit)
- Warburg Micro syndrome (links | edit)
- Weill–Marchesani syndrome (links | edit)
- Hereditary carrier (links | edit)
- Central core disease (links | edit)
- Antley–Bixler syndrome (links | edit)
- Homeobox protein goosecoid (links | edit)
- Hypoalphalipoproteinemia (links | edit)
- Posterior spinal artery syndrome (links | edit)
- Renal–hepatic–pancreatic dysplasia (links | edit)
- Afro-Jamaicans (links | edit)
- 6-phosphogluconate dehydrogenase deficiency (links | edit)
- Obligate carrier (links | edit)
- Ocular albinism type 1 (links | edit)
- Joseph Paruta (links | edit)
- Schindler disease (links | edit)
- Diplopodia (links | edit)
- Blau syndrome (links | edit)
- Tetra-amelia syndrome (links | edit)
- Kalash people (links | edit)
- Acytosiosis (links | edit)
- Marinesco–Sjögren syndrome (links | edit)
- Virtual karyotype (links | edit)
- Blue budgerigar mutation (links | edit)
- Dominant Grey budgerigar mutation (links | edit)
- Violet budgerigar mutation (links | edit)
- Greywing budgerigar mutation (links | edit)
- Dominant Clearbody budgerigar mutation (links | edit)
- English Fallow budgerigar mutation (links | edit)
- Scottish Fallow budgerigar mutation (links | edit)
- Finnish heritage disease (links | edit)
- Nager acrofacial dysostosis (links | edit)
- Accessory auricle (links | edit)
- Scrambler mouse (links | edit)
- Behavioural genetics (links | edit)
- Neuroferritinopathy (links | edit)
- Singleton Merten syndrome (links | edit)
- Lethal arthrogryposis with anterior horn cell disease (links | edit)
- Scalp–ear–nipple syndrome (links | edit)
- Genetic history of the Indigenous peoples of the Americas (links | edit)
- Clearflight Pied budgerigar mutation (links | edit)
- Australian Pied budgerigar mutation (links | edit)
- Roberts syndrome (links | edit)
- Copper in biology (links | edit)
- Argininemia (links | edit)
- Neuromechanics of idiopathic scoliosis (links | edit)
- BZIP Maf (links | edit)
- Minuet cat (links | edit)
- Donohue syndrome (links | edit)
- Katz syndrome (links | edit)
- Pontocerebellar hypoplasia (links | edit)
- PHACE syndrome (links | edit)
- Beare–Stevenson cutis gyrata syndrome (links | edit)
- Genetic studies on Arabs (links | edit)
- Chromosomal deletion syndrome (links | edit)
- Eiken syndrome (links | edit)
- Dicarboxylic aminoaciduria (links | edit)
- Tricho–dento–osseous syndrome (links | edit)
- Hereditary gingival fibromatosis (links | edit)
- NUBPL (links | edit)
- Opitz G/BBB syndrome (links | edit)
- Sanjad–Sakati syndrome (links | edit)
- Jōmon period (links | edit)
- Mezhovskaya culture (links | edit)
- Ann T. Bowling (links | edit)
- Genetic studies on Bulgarians (links | edit)
- Genome-wide complex trait analysis (links | edit)
- Ataxia-pancytopenia syndrome (links | edit)
- Nevo syndrome (links | edit)
- International System for Human Cytogenomic Nomenclature (links | edit)
- Hyperinsulinism-hyperammonemia syndrome (links | edit)
- Cetina culture (links | edit)
- Genetic studies on Filipinos (links | edit)
- Hyperkalemic periodic paralysis (equine) (links | edit)
- Māori history (links | edit)
- Sarcophaga barbata (links | edit)
- Mitochondrial complex II deficiency (links | edit)
- Fibroblastic and myofibroblastic tumors (links | edit)
- Haptoglobin-related protein (links | edit)
- Talk:Khoisan (links | edit)
- Talk:Latvians (links | edit)
- Talk:Roan (color) (links | edit)
- Talk:Sex linkage (links | edit)
- Talk:Irish people/Archive 1 (links | edit)
- Talk:Race and genetics/Archive 1 (links | edit)
- Talk:Dalit/ Archive 1 (links | edit)
- Talk:Dravidian peoples/Archive 1 (links | edit)
- Talk:Prehistory of the Philippines (links | edit)
- Talk:Finnish heritage disease (links | edit)
- Talk:Scottish people/Archive 3 (links | edit)
- Talk:Genetics and archaeogenetics of South Asia/Archive 3 (links | edit)
- Talk:Irish people/Archive 4 (links | edit)
- Talk:Spaniards/Archive 7 (links | edit)
- Talk:Neutropenia/Archive 1 (links | edit)
- Talk:Turkish people/Archive 16 (links | edit)
- Talk:Corded Ware culture/Archive 1 (links | edit)
- User:Alteripse/workshop2 (links | edit)
- User:Dr d12 (links | edit)
- User:CALR/Words (links | edit)
- User:Dodo bird/Temp (links | edit)
- User:Enviromet/Subpage 1 Copper in health - working draft (links | edit)
- User:Michelllin198666/sandbox (links | edit)
- User:Benutzer41/sidscopy (links | edit)
- User:Moutasem z/sandbox (links | edit)
- User:Lucialemon/sandbox (links | edit)
- User:Lszleszynski/sandbox (links | edit)
- User:SaswatPanda/Genetic Basis of the Osteochondrodysplasias (links | edit)
- User:WeijiBaikeBianji/sandbox24 (links | edit)
- User:KateSage/sandbox (links | edit)
- User:LaurenNicole7911/sandbox (links | edit)
- User:Julrich88/sandbox (links | edit)
- User:Ricov53/sandbox (links | edit)
- User:Acer/Simple1 (links | edit)
- User:Tbechar/sandbox (links | edit)
- User:Ashah211/sandbox (links | edit)
- User:Sgilyard/sandbox (links | edit)
- User:Rsscience/sandbox (links | edit)
- User:Rhawley10/sandbox (links | edit)
- User:Hganev/sandbox (links | edit)
- User:Egeorge01/sandbox (links | edit)
- User:Karp246/sandbox (links | edit)
- User:Nthaiba/sandbox (links | edit)
- User:Grimhelm/Irish people (links | edit)
- User:Aherrera09/sandbox (links | edit)
- User:Coolheli/sandbox (links | edit)
- User:Journee Williams/sandbox (links | edit)
- User:Dmil3422/Laron Syndrome (links | edit)
- User:King-Joma/Ataxia (links | edit)
- User:Jmrpuls/GAMT sandbox (links | edit)
- User talk:Jessicanr (links | edit)
- User talk:Middayexpress/Archive 18 (links | edit)
- Wikipedia:Reference desk/Archives/Humanities/2008 November 29 (links | edit)
- Wikipedia:Reference desk/Archives/Science/2009 February 7 (links | edit)
- Wikipedia:Reference desk/Archives/Science/2009 April 1 (links | edit)
- Wikipedia:Categories for discussion/Log/2023 December 29 (links | edit)
- Template:Transclude list item excerpts as random slideshow/testcases/Portal:Lithuania (links | edit)
- Category:Genetic genealogy companies (links | edit)
- Cenani–Lenz syndactylism (links | edit)
- Early modern human (links | edit)