MeSH term
Frequency | Condition_Probility | Animals | 10 | 0.0 |
Cell Line | 6 | 0.0 |
Humans | 40 | 0.0 |
Research Support, Non-U.S. Gov't | 17 | 0.0 |
Research Support, U.S. Gov't, P.H.S. | 16 | 0.0 |
Cloning, Molecular | 3 | 0.0 |
Comparative Study | 6 | 0.0 |
Kinetics | 2 | 0.0 |
Substrate Specificity | 2 | 0.0 |
Male | 26 | 0.0 |
Child | 11 | 0.0 |
Child, Preschool | 7 | 0.0 |
Infant | 4 | 0.0 |
Linkage (Genetics)/genetics | 3 | 1.0 |
Oculocerebrorenal Syndrome/*diagnosis/genetics | 2 | 100.0 |
Phosphatidylinositol 4,5-Diphosphate/metabolism | 3 | 10.0 |
X Chromosome | 2 | 0.0 |
Oculocerebrorenal Syndrome/*genetics | 14 | 93.0 |
*Phosphoric Monoester Hydrolases | 6 | 13.0 |
Polymerase Chain Reaction | 6 | 0.0 |
Proteins/*genetics | 11 | 0.0 |
Adult | 11 | 0.0 |
Blotting, Western | 3 | 0.0 |
Fibroblasts/enzymology | 2 | 1.0 |
Oculocerebrorenal Syndrome/*diagnosis | 3 | 100.0 |
Alternative Splicing | 2 | 0.0 |
DNA Mutational Analysis | 6 | 0.0 |
Female | 12 | 0.0 |
Sequence Deletion | 5 | 0.0 |
Adolescent | 9 | 0.0 |
Amino Acid Sequence | 9 | 0.0 |
Base Sequence | 7 | 0.0 |
Molecular Sequence Data | 13 | 0.0 |
Mutation | 4 | 0.0 |
Pedigree | 6 | 0.0 |
Phosphoric Monoester Hydrolases | 2 | 33.0 |
Genetic Screening | 3 | 0.0 |
Sequence Homology, Amino Acid | 2 | 0.0 |
Blotting, Northern | 3 | 0.0 |
Cells, Cultured | 4 | 0.0 |
Phosphoric Monoester Hydrolases/*genetics | 4 | 1.0 |
Sequence Analysis, DNA | 2 | 0.0 |
Exons | 2 | 0.0 |
Fibroblasts | 2 | 0.0 |
Frameshift Mutation | 2 | 0.0 |
Lymphocytes | 2 | 1.0 |
*Mutation | 3 | 0.0 |
Point Mutation | 2 | 0.0 |
Polymorphism, Single-Stranded Conformational | 2 | 0.0 |
Mutation/*genetics | 2 | 0.0 |
Phenotype | 2 | 0.0 |
Mice | 3 | 0.0 |
Oculocerebrorenal Syndrome/*genetics/physiopathology | 2 | 100.0 |
Fluorescent Antibody Technique, Indirect | 2 | 0.0 |
DNA Primers | 2 | 0.0 |
Research Support, U.S. Gov't, Non-P.H.S. | 2 | 0.0 |
Sequence Alignment | 2 | 0.0 |
Protein Biosynthesis | 2 | 0.0 |
Aggression | 2 | 16.0 |
Stereotyped Behavior | 2 | 22.0 |
*X Chromosome | 6 | 0.0 |
Polymorphism, Genetic | 2 | 0.0 |
Gene Library | 2 | 0.0 |
Linkage (Genetics) | 2 | 0.0 |
Translocation, Genetic | 2 | 0.0 |
Blotting, Southern | 3 | 0.0 |
Chromosome Mapping | 2 | 0.0 |
Hybrid Cells | 2 | 0.0 |
