| cystic, fibrosis, cf, patients, mutations, screening, cftr, gene, disease, mutation, diagnosis, clinical, pancreatic, genetic, one, carrier, pancreatitis, testing, two, associated |
carrier screening, carrier testing, cf patients, cftr gene, cystic fibrosis gene carrier, disease-associated mutations |
| gene, deafness, mutations, mutation, cx26, hearing, loss, cells, genetic, connexin, gjb2, syndrome, 35delg, recessive, human, cases, congenital, two, children, protein |
cx26 gene mutations, gjb2 gene, hearing loss, mutations 35delg, two cases |
| syndrome, x, autism, disorders, fragile, disorder, genetic, gene, mental, retardation, patients, developmental, clinical, chromosome, genes, study, autistic, associated, children, behavioral |
autistic disorder, developmental disorders, fragile x chromosome syndrome, fragile x mental retardation gene, fragile x syndrome, fragile x-associated disorders, fragile-x mental retardation syndrome, mental disorder |
| mutations, cardiomyopathy, hypertrophic, hcm, cardiac, mutation, patients, gene, myosin, protein, familial, disease, chain, heart, genetic, genes, c, human, results, troponin |
cardiac myosin, cardiac troponin c, familial hypertrophic cardiomyopathy mutations, heart disease |
