MeSH term
Frequency | Condition_Probility | Child | 4 | 0.0 |
Female | 16 | 0.0 |
Humans | 24 | 0.0 |
Syndrome | 19 | 1.0 |
Abnormalities, Multiple/*genetics | 5 | 1.0 |
Chromosome Mapping | 9 | 0.0 |
Chromosomes, Human, Pair 1/*genetics | 5 | 2.0 |
Cleft Lip/*genetics | 15 | 24.0 |
Cleft Palate/*genetics | 17 | 23.0 |
Lip/*abnormalities | 3 | 100.0 |
Lod Score | 6 | 0.0 |
Male | 14 | 0.0 |
Pedigree | 15 | 0.0 |
Polymorphism, Genetic | 2 | 0.0 |
Research Support, Non-U.S. Gov't | 15 | 0.0 |
Alleles | 2 | 0.0 |
Animals | 3 | 0.0 |
Base Sequence | 4 | 0.0 |
Haplotypes/genetics | 2 | 0.0 |
Molecular Sequence Data | 5 | 0.0 |
Polymorphism, Genetic/*genetics | 2 | 0.0 |
Research Support, U.S. Gov't, P.H.S. | 9 | 0.0 |
Cleft Lip/*genetics/pathology | 2 | 28.0 |
DNA Mutational Analysis | 3 | 0.0 |
Adult | 5 | 0.0 |
*Chromosomes, Human, Pair 1 | 6 | 1.0 |
Cleft Lip/genetics | 2 | 22.0 |
Cleft Palate/genetics | 2 | 8.0 |
*Linkage (Genetics) | 3 | 0.0 |
Penetrance | 3 | 2.0 |
Anodontia/*genetics | 4 | 22.0 |
Genetic Markers | 4 | 0.0 |
Chromosomes, Human, Pair 1 | 2 | 0.0 |
Genes, Dominant | 3 | 0.0 |
*Mutation | 3 | 0.0 |
Infant, Newborn | 2 | 0.0 |
DNA, Satellite/genetics | 2 | 1.0 |
Lip/abnormalities | 2 | 66.0 |
*Sequence Deletion | 2 | 0.0 |
Polymerase Chain Reaction | 2 | 0.0 |
DNA-Binding Proteins/*genetics | 4 | 0.0 |
Mutation, Missense | 2 | 0.0 |
Transcription Factors/*genetics | 4 | 0.0 |
China | 2 | 0.0 |
