MeSH term
Frequency | Condition_Probility | Biopsy | 5 | 0.0 |
Child | 8 | 0.0 |
Child, Preschool | 5 | 0.0 |
Humans | 25 | 0.0 |
Immunohistochemistry | 6 | 0.0 |
Male | 16 | 0.0 |
Muscle, Skeletal/pathology | 3 | 5.0 |
Muscular Dystrophies/congenital/*genetics/pathology | 3 | 100.0 |
Mutation | 3 | 0.0 |
Phenotype | 3 | 0.0 |
Research Support, Non-U.S. Gov't | 25 | 0.0 |
Research Support, U.S. Gov't, P.H.S. | 3 | 0.0 |
Family Health | 2 | 0.0 |
Female | 15 | 0.0 |
Haplotypes | 3 | 0.0 |
Pedigree | 10 | 0.0 |
Infant | 4 | 0.0 |
Laminin/*deficiency | 2 | 100.0 |
Adult | 3 | 0.0 |
Consanguinity | 6 | 1.0 |
DNA Mutational Analysis | 4 | 0.0 |
Laminin/*genetics | 4 | 9.0 |
Chromosome Mapping | 8 | 0.0 |
Linkage (Genetics)/genetics | 2 | 0.0 |
Magnetic Resonance Imaging | 4 | 0.0 |
Animals | 4 | 0.0 |
Mice | 3 | 0.0 |
Muscular Dystrophies/*congenital/*genetics | 4 | 80.0 |
Linkage (Genetics) | 5 | 0.0 |
DNA Primers | 3 | 0.0 |
Exons | 2 | 0.0 |
Introns | 2 | 0.0 |
Microsatellite Repeats | 2 | 0.0 |
Polymerase Chain Reaction | 2 | 0.0 |
Polymorphism, Single-Stranded Conformational | 2 | 0.0 |
*Prenatal Diagnosis | 3 | 1.0 |
Sequence Analysis, DNA | 2 | 0.0 |
Laminin/deficiency/*genetics | 2 | 100.0 |
Muscular Dystrophies/congenital/*diagnosis/*genetics | 2 | 100.0 |
Genetic Markers | 2 | 0.0 |
Pregnancy | 3 | 0.0 |
Amino Acid Sequence | 5 | 0.0 |
Base Sequence | 5 | 0.0 |
Conserved Sequence | 3 | 0.0 |
Fluorescent Antibody Technique | 2 | 0.0 |
Molecular Sequence Data | 5 | 0.0 |
Laminin/*deficiency/*genetics | 3 | 75.0 |
*Chromosomes, Human, Pair 6 | 4 | 1.0 |
Homozygote | 3 | 0.0 |
Comparative Study | 2 | 0.0 |
Drosophila | 2 | 0.0 |
Sequence Homology, Amino Acid | 2 | 0.0 |
Brain/pathology | 3 | 0.0 |
