MeSH term
Frequency | Condition_Probility | *Chromosome Deletion | 2 | 0.0 |
Female | 3 | 0.0 |
Humans | 10 | 0.0 |
Male | 2 | 0.0 |
Oligonucleotide Array Sequence Analysis | 2 | 0.0 |
Research Support, Non-U.S. Gov't | 9 | 0.0 |
Base Sequence | 4 | 0.0 |
Cells, Cultured | 2 | 0.0 |
*Chromosomes, Human, Pair 17 | 3 | 0.0 |
Evolution, Molecular | 2 | 0.0 |
Gene Duplication | 2 | 1.0 |
Molecular Sequence Data | 6 | 0.0 |
Neurofibromatosis 1/*genetics | 4 | 2.0 |
Sequence Homology, Nucleic Acid | 3 | 0.0 |
Chromosomes, Human, Pair 17 | 2 | 0.0 |
Exons | 3 | 0.0 |
*Gene Deletion | 2 | 0.0 |
Nerve Tissue Proteins/*genetics | 2 | 0.0 |
Phenotype | 2 | 0.0 |
Adolescent | 2 | 0.0 |
Adult | 3 | 0.0 |
Child | 2 | 0.0 |
Child, Preschool | 3 | 0.0 |
*Gene Expression Regulation, Neoplastic | 2 | 0.0 |
*Genes, Neurofibromatosis 1 | 4 | 2.0 |
Introns | 2 | 0.0 |
Research Support, U.S. Gov't, P.H.S. | 3 | 0.0 |
Animals | 4 | 0.0 |
Amino Acid Sequence | 2 | 0.0 |
Mice | 3 | 0.0 |
