MeSH term
Frequency | Condition_Probility | Adolescent | 3 | 0.0 |
*Chromosome Deletion | 2 | 0.0 |
Chromosomes, Human, Pair 8/*genetics | 2 | 1.0 |
Humans | 24 | 0.0 |
Male | 11 | 0.0 |
Microsatellite Repeats | 3 | 0.0 |
Amino Acid Sequence | 3 | 0.0 |
Ankyrins/*genetics | 6 | 60.0 |
Base Sequence | 9 | 0.0 |
English Abstract | 2 | 0.0 |
Female | 12 | 0.0 |
Molecular Sequence Data | 10 | 0.0 |
Research Support, Non-U.S. Gov't | 18 | 0.0 |
Adult | 4 | 0.0 |
Aged | 2 | 0.0 |
Animals | 3 | 0.0 |
Mice | 2 | 0.0 |
Pedigree | 6 | 0.0 |
Spherocytosis, Hereditary/*genetics | 6 | 60.0 |
Family Health | 2 | 0.0 |
Child | 2 | 0.0 |
*Mutation | 2 | 0.0 |
Polymerase Chain Reaction | 5 | 0.0 |
RNA, Messenger/analysis | 2 | 0.0 |
Exons/genetics | 2 | 0.0 |
*Frameshift Mutation | 2 | 1.0 |
Research Support, U.S. Gov't, P.H.S. | 5 | 0.0 |
RNA, Messenger/genetics | 2 | 0.0 |
Ankyrins/*metabolism | 3 | 50.0 |
Binding Sites | 2 | 0.0 |
Cell Line | 3 | 0.0 |
Sequence Homology, Amino Acid | 2 | 0.0 |
Mutation | 4 | 0.0 |
Polymorphism, Genetic | 3 | 0.0 |
Blood Proteins/*genetics | 2 | 1.0 |
Membrane Proteins/*genetics | 2 | 0.0 |
Heterozygote | 3 | 0.0 |
Werner Syndrome/*genetics | 3 | 10.0 |
Breast Neoplasms/*genetics | 2 | 0.0 |
*Chromosomes, Human, Pair 8 | 6 | 2.0 |
Oligodeoxyribonucleotides | 2 | 0.0 |
Protein Binding | 2 | 0.0 |
Chromosome Mapping | 4 | 0.0 |
Genetic Markers | 4 | 0.0 |
DNA | 2 | 0.0 |
Linkage (Genetics) | 2 | 0.0 |
Gene Frequency | 2 | 0.0 |
Lod Score | 2 | 0.0 |
Membrane Proteins/genetics | 2 | 0.0 |
