MeSH term
Frequency | Condition_Probility | Animals | 12 | 0.0 |
Humans | 33 | 0.0 |
Amino Acid Sequence | 6 | 0.0 |
Base Sequence | 7 | 0.0 |
DNA/genetics | 4 | 0.0 |
Female | 13 | 0.0 |
Genes, Dominant | 3 | 0.0 |
Male | 14 | 0.0 |
Molecular Sequence Data | 7 | 0.0 |
Mutation | 13 | 0.0 |
Pedigree | 6 | 0.0 |
Research Support, Non-U.S. Gov't | 23 | 0.0 |
Sequence Homology, Amino Acid | 2 | 0.0 |
Mice | 7 | 0.0 |
Mice, Inbred C57BL | 3 | 0.0 |
Phenotype | 12 | 0.0 |
Proteins/*genetics | 19 | 1.0 |
Research Support, U.S. Gov't, P.H.S. | 15 | 0.0 |
Cell Division | 2 | 0.0 |
Infant | 3 | 0.0 |
Proteins/genetics/metabolism | 3 | 1.0 |
Alagille Syndrome/*genetics | 11 | 73.0 |
Alagille Syndrome/*genetics/pathology | 5 | 83.0 |
Child, Preschool | 3 | 0.0 |
Chromosomes, Human, Pair 20/*genetics | 3 | 5.0 |
In Situ Hybridization, Fluorescence | 3 | 0.0 |
DNA/chemistry/genetics | 2 | 0.0 |
DNA Mutational Analysis | 6 | 0.0 |
Family Health | 4 | 0.0 |
Genotype | 4 | 0.0 |
Polymorphism, Single-Stranded Conformational | 5 | 0.0 |
Severity of Illness Index | 2 | 0.0 |
DNA Primers | 2 | 0.0 |
*Mutation | 7 | 0.0 |
Chromosome Mapping | 4 | 0.0 |
Homozygote | 2 | 0.0 |
Mutation, Missense | 4 | 0.0 |
Rats | 2 | 0.0 |
Sequence Analysis, DNA | 3 | 0.0 |
Heterozygote | 2 | 0.0 |
Proteins/*genetics/metabolism | 2 | 0.0 |
Gene Expression Regulation, Developmental | 2 | 0.0 |
In Situ Hybridization | 3 | 0.0 |
Membrane Proteins/*genetics | 2 | 0.0 |
Diagnosis, Differential | 2 | 0.0 |
Genetic Markers | 2 | 0.0 |
*Chromosome Deletion | 2 | 0.0 |
Child | 5 | 0.0 |
Gene Deletion | 6 | 0.0 |
Proteins/genetics | 3 | 0.0 |
DNA Primers/genetics | 2 | 0.0 |
Frameshift Mutation | 3 | 0.0 |
RNA Splicing/genetics | 3 | 2.0 |
Sequence Deletion | 3 | 0.0 |
*Transcription Factors | 3 | 0.0 |
Chromosomes, Human, Pair 20/genetics | 2 | 7.0 |
Cloning, Molecular | 2 | 0.0 |
Exons/genetics | 2 | 0.0 |
Introns/genetics | 2 | 0.0 |
*Receptors, Cell Surface | 2 | 0.0 |
Adult | 2 | 0.0 |
Alagille Syndrome/*diagnosis/*genetics | 2 | 100.0 |
