MeSH term
Frequency | Condition_Probility | Carrier Proteins/*genetics | 9 | 0.0 |
*Chromosome Aberrations | 2 | 0.0 |
Chromosome Banding | 2 | 0.0 |
Chromosomes, Human, Pair 15/*genetics | 3 | 3.0 |
Female | 18 | 0.0 |
Humans | 44 | 0.0 |
In Situ Hybridization, Fluorescence | 3 | 0.0 |
Membrane Proteins/*genetics | 11 | 1.0 |
*Membrane Transport Proteins | 18 | 3.0 |
Middle Aged | 3 | 0.0 |
Research Support, Non-U.S. Gov't | 28 | 0.0 |
*Membrane Glycoproteins | 3 | 0.0 |
*Oxidoreductases | 5 | 6.0 |
Pigmentation/*genetics | 3 | 27.0 |
Polymorphism, Genetic | 2 | 0.0 |
Receptors, Melanocortin | 2 | 2.0 |
Variation (Genetics) | 3 | 0.0 |
Adult | 12 | 0.0 |
Alleles | 10 | 0.0 |
Amino Acid Sequence | 5 | 0.0 |
Animals | 10 | 0.0 |
Child, Preschool | 9 | 0.0 |
Cloning, Molecular | 4 | 0.0 |
DNA Mutational Analysis | 3 | 0.0 |
Exons/genetics | 3 | 0.0 |
Homozygote | 3 | 0.0 |
Male | 22 | 0.0 |
*Membrane Proteins | 2 | 0.0 |
Mice | 7 | 0.0 |
Molecular Sequence Data | 10 | 0.0 |
Mutation/*genetics | 5 | 0.0 |
Pigmentation/genetics | 4 | 33.0 |
Research Support, U.S. Gov't, P.H.S. | 24 | 0.0 |
Sequence Alignment | 2 | 0.0 |
Albinism, Oculocutaneous/*genetics | 10 | 55.0 |
Carrier Proteins/*genetics/metabolism | 3 | 1.0 |
Membrane Proteins/*genetics/metabolism | 3 | 1.0 |
African Continental Ancestry Group/genetics | 6 | 2.0 |
Chromosome Mapping | 3 | 0.0 |
*Chromosomes, Human, Pair 15 | 5 | 2.0 |
Genetic Markers | 2 | 0.0 |
Haplotypes | 4 | 0.0 |
Lod Score | 2 | 0.0 |
Monophenol Monooxygenase/*genetics | 4 | 16.0 |
Pedigree | 4 | 0.0 |
Sequence Deletion | 5 | 0.0 |
South Africa | 2 | 1.0 |
Africa South of the Sahara | 2 | 13.0 |
Amino Acid Substitution | 2 | 0.0 |
Gene Frequency | 5 | 0.0 |
Genotype | 5 | 0.0 |
Phenotype | 9 | 0.0 |
Polymorphism, Single-Stranded Conformational | 4 | 0.0 |
Variation (Genetics)/genetics | 2 | 1.0 |
Eye Color/*genetics | 2 | 50.0 |
Angelman Syndrome/*genetics | 3 | 6.0 |
*Chromosome Deletion | 2 | 0.0 |
*Multigene Family | 2 | 0.0 |
Prader-Willi Syndrome/*genetics | 2 | 2.0 |
Base Sequence | 9 | 0.0 |
African Continental Ancestry Group/*genetics | 2 | 0.0 |
Albinism, Oculocutaneous/classification/*genetics | 3 | 100.0 |
DNA Primers | 3 | 0.0 |
Mutation | 6 | 0.0 |
Polymerase Chain Reaction | 8 | 0.0 |
Proteins/*genetics | 2 | 0.0 |
*Gene Deletion | 6 | 0.0 |
Zimbabwe | 2 | 7.0 |
Adolescent | 6 | 0.0 |
Child | 9 | 0.0 |
Heterozygote | 6 | 0.0 |
Membrane Proteins/genetics | 3 | 0.0 |
Prevalence | 3 | 0.0 |
Socioeconomic Factors | 2 | 1.0 |
Monophenol Monooxygenase/genetics | 3 | 14.0 |
Melanocytes/metabolism | 2 | 5.0 |
Infant | 5 | 0.0 |
*Mutation | 3 | 0.0 |
Cell Line | 2 | 0.0 |
Comparative Study | 5 | 0.0 |
Cells, Cultured | 2 | 0.0 |
Exons | 3 | 0.0 |
*Sequence Deletion | 2 | 0.0 |
Twins, Dizygotic | 2 | 5.0 |
Albinism, Oculocutaneous/ethnology/*genetics | 2 | 66.0 |
Ethnic Groups/genetics | 2 | 1.0 |
Infant, Newborn | 3 | 0.0 |
Japan | 2 | 0.0 |
Africa/ethnology | 2 | 4.0 |
Monophenol Monooxygenase/*genetics/metabolism | 2 | 66.0 |
Chromosomes, Human, Pair 15/genetics | 2 | 2.0 |
Hair Color/genetics | 2 | 11.0 |
Linkage Disequilibrium | 2 | 0.0 |
