Pages that link to "Autosome"
← Autosome
The following pages link to Autosome:
Displaying 50 items.
- Wikipedia:WikiProject Molecular and Cellular Biology/Style guidelines (← links)
- Chromatin (← links)
- List of molecular biology topics (← links)
- Infantile neuronal ceroid lipfuscinosis (← links)
- Congenital disorder (← links)
- Glycogen storage disease type VII (← links)
- Lipid storage disorder (← links)
- Mevalonic aciduria (← links)
- Cerebellar abiotrophy (← links)
- Recessive gene (← links)
- Zimmerman-Laband syndrome (← links)
- Human (← links)
- ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities (← links)
- List of ICD-9 codes 740-759: Congenital anomalies (← links)
- Chromosome 5 (← links)
- LPL (← links)
- Chromosome 19 (← links)
- Chromosome 9 (← links)
- Chromosome 4 (← links)
- Chromosome 1 (← links)
- Chromosome 7 (← links)
- Chromosome 18 (← links)
- Chromosome 17 (← links)
- Chromosome 12 (← links)
- Chromosome 6 (← links)
- Chromosome 2 (← links)
- Chromosome 11 (← links)
- Chromosome 3 (← links)
- The WikiDoc Living Textbook of Genetics (← links)
- Sexual differentiation (← links)
- Cell growth (← links)
- Synapsis (← links)
- Autosomes (redirect page) (← links)
- ICD-10 Chapter Q (← links)
- Human evolutionary genetics (← links)
- Homologous chromosome (← links)
- HLA-DQ2 (← links)
- ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities (← links)
- Sexual dimorphism (← links)
- Sex differences in humans (← links)
- Gluten immunochemistry (← links)
- WBR0119 (← links)
- Gonadoblastoma pathophysiology (← links)
- Autosomal (redirect page) (← links)
- Karyotype (← links)
- Neuroendocrine tumors (← links)
- OMIM (← links)
- Aceruloplasminemia (← links)
- ICD-10 Chapter Q (← links)
- Mendelian Inheritance in Man (← links)
- Saethre-Chotzen syndrome (← links)
- Oguchi disease (← links)
- Ablepharon macrostomia syndrome (← links)
- Acheiropodia (← links)
- Acrodermatitis enteropathica (← links)
- Adenylosuccinate lyase deficiency (← links)
- Alpha-mannosidosis (← links)
- Keratoconus (← links)
- Heterochromia (← links)
- Kjer's optic neuropathy (← links)
- Becker's muscular dystrophy (← links)
- Biological inheritance (← links)
- Human genome (← links)
- Reciprocal cross (← links)
- Hardy-Weinberg principle (← links)
- Genealogical DNA test (← links)
- Sorenson foundation (← links)
- Genetics and Archaeogenetics of South Asia (← links)
- Abderhalden-Kaufmann-Lignac syndrome (← links)
- Crigler-Najjar syndrome (← links)
- Diastrophic dysplasia (← links)
- Glutathione synthetase deficiency (← links)
- Guanidinoacetate methyltransferase deficiency (← links)
- Hyperkalemic periodic paralysis (← links)
- Hyperlysinemia (← links)
- Nonsyndromic deafness (← links)
- Pachyonychia congenita (← links)
- Prolidase deficiency (← links)
- Sarcosinemia (← links)
- Succinic semialdehyde dehydrogenase deficiency (← links)
- Genomic imprinting (← links)
- Phosphogluconate dehydrogenase (← links)
- Glycogen branching enzyme (← links)
- Arginase (← links)
- ACADSB (← links)
- Arylsulfatase A (← links)
- Pseudoautosomal region (← links)
- Heterozygote advantage (← links)
- Sitosterolemia (← links)
- Phosphoglycerate kinase (← links)
- Aldolase A (← links)
- White sponge nevus (← links)
- Asparagine (← links)
- Cystic medial necrosis (← links)
- Zaspopathy (← links)
- Familial dysfibrinogenemia (← links)
- Marinesco-Sjogren syndrome (← links)
- Zori Stalker Williams syndrome (← links)
- Gerstmann-Sträussler-Scheinker syndrome (← links)
- Wolman disease (← links)
- Sabinas brittle hair syndrome (← links)
- ICF syndrome (← links)
- Lafora disease (← links)
- Limb-girdle muscular dystrophy (← links)
- Meleda Disease (← links)
- Miller-Dieker syndrome (← links)
- Rapadilino syndrome (← links)
- Mucolipidosis (← links)
- Centronuclear myopathy (← links)
- Pantothenate kinase-associated neurodegeneration (← links)
- Donohue syndrome (← links)
- Nezelof syndrome (← links)
- Zimmerman-Laband syndrome (← links)
- Yunis-Varon syndrome (← links)
- Hematidrosis (← links)
- ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities (← links)
- The WikiDoc Living Textbook of Genetics (← links)
- Causes and origins of Tourette syndrome (← links)
- Monosomy (← links)
- Combined immunodeficiency (← links)
- Axenfeld syndrome (← links)
- Cri du chat syndrome (← links)
- Intraflagellar transport (← links)
- Branchio-oto-renal syndrome (← links)
- Keutel syndrome (← links)
- NT5C3 (← links)
- CHKB (gene) (← links)
- Central core disease (← links)
- Antley-Bixler syndrome (← links)
- Trimethylamine (← links)
- Rothmund-Thomson syndrome (← links)
- Carnosinemia (← links)
- Pelger-Huet anomaly (← links)
- Acute intermittant porphyria (← links)
- Gunther disease (← links)
- Micro syndrome (← links)
- Argininemia (← links)
- Tetrasomy (← links)
- Infantile free sialic acid storage disease (← links)
- Papillon-Lefevre syndrome (← links)
- Acrocallosal syndrome (← links)
- Weill-Marchesani syndrome (← links)
- Congenital adrenal hyperplasia overview (← links)
- Glucagonoma differential diagnosis (← links)
- 17-beta-hydroxysteroid dehydrogenase deficiency overview (← links)
- 17-beta-hydroxysteroid dehydrogenase deficiency historical perspective (← links)
- Thrombotic thrombocytopenic purpura classification (← links)
- Hemophilia classification (← links)
- Hemophilia epidemiology and demographics (← links)
- Hemophilia pathophysiology (← links)
- Hemophilia A overview (← links)
- Sideroblastic anemia classification (← links)
- Von Willebrand disease classification (← links)
- Papillorenal syndrome overview (← links)
- Thin basement membrane disease pathophysiology (← links)
- Thin basement membrane disease overview (← links)
- Thin basement membrane disease historical perspective (← links)
- Hurler syndrome pathophysiology (← links)
- Alstrom syndrome pathophysiology (← links)
- Hyperhidrosis history and symptoms (← links)
- WBR0111 (← links)
- WBR0120 (← links)
- WBR0544 (← links)
- Galactosemia overview (← links)
- Galactosemia causes (← links)
- Galactosemia primary prevention (← links)
- WBR0117 (← links)
- Sandbox simrat (← links)
- Schindler disease (← links)
- Pontocerebellar hypoplasia (← links)
- Roberts syndrome (← links)
- Sandbox cah 17 (← links)
- Hartnup Disease overview (← links)
- Hartnup Disease causes (← links)
- Hartnup Disease pathophysiology (← links)
- Propionic acidemia overview (← links)
- Propionic acidemia pathophysiology (← links)
- Propionic acidemia epidemiology and demographics (← links)
- Glanzmann's thrombasthenia causes (← links)
- Glanzmann's thrombasthenia overview (← links)
- Uridine triacetate (← links)
- Proteoglycan 4 (← links)
- NUBPL (← links)
- Sudden infant death syndrome classification (← links)
- Galactosemia Risk factors (← links)
- Template:Chromosomal abnormalities (← links)
- Nucleosome (← links)
- Chromosome 15 (← links)
- Chromosome 13 (← links)
- Chromosome 14 (← links)
- Chromosome 8 (← links)
- Chromosome 21 (← links)
- Pancreatic disease (← links)
- Chromosome 10 (← links)
- Chromosome 16 (← links)
- Caenorhabditis elegans (← links)
- Drosophila melanogaster (← links)
- CENPJ (← links)
- CENPC1 (← links)
- CENPH (← links)
- CENPI (← links)
- CENPM (← links)