transcriptional initiation site / cellular machinery / particular chromosomal site / chemical modification / detectable β-globin product / gene product / on-line version / splice acceptor site / in vitro and prokaryotic systems / /
MedicalCondition
Ehlers-Danlos syndrome / adolescent cancer / MULTIFACTORIAL DISEASES / ovarian cancers / muscular dystrophy / skin blistering disease / Li-Fraumeni syndrome / Autosomal recessive diseases / exocrine pancreatic and pulmonary functions / Apert syndrome / retinoblastoma / seizures / MENDELIAN DISEASES / Charcot-Marie-Tooth disease type / severe mental retardation / phenotypically different and more severe thanatophoric dwarfism / Hereditary colorectal cancers / OF MENDELIAN DISEASES / Essential hypertension / given disease / Isolated congenital abnormalities / craniofacial abnormalities / clinical disease / Dejerine-Sottas disease / pressure palsies / Prader-Willi syndrome / A. CONGENITAL ABNORMALITIES / Autosomal dominant diseases / well-known recessive disease / associated disease / cystic fibrosis gene / inducible genetic disease / lung disease / obesity / designation cystic fibrosis / Jackson-Weiss syndrome / hypertrophic demyelinating peripheral neuropathy / simple Mendelian diseases / such diseases / achondroplasia / CFTR cystic fibrosis / Coronary heart disease / Osteogenesis imperfecta / C. COMMON MULTIFACTORIAL DISEASES / peripheral neuropathies / familial hypercholesterolemia / cystic fibrosis / single-gene disorder / severe disease / certain genetic diseases / clinical diseases / Mendelian disease / human Mendelian diseases / such genetic diseases / ataxia / intestinal obstruction / thanatophoric dysplasia / X-linked diseases / breast cancers / Hereditary / Ataxia-telangiectasia / CANCER / Genetic disease / osteogenesis imperfecta I / disease / FOR GENETIC DISEASES / lengthmutation-associated diseases / haemophilia B / achondroplasia / thanatophoric dwarfism / genetic diseases / pulmonary disease / FOR MULTIFACTORIAL DISEASES / least two other craniosynostosis syndrome / epidermolysis bullosa dystropica / hereditary neuropathy / pancreatic insufficiency / Pfeiffer syndrome / hereditary effects / Angelman syndrome / Wolf-Hirschhorn syndrome / Diabetes mellitus / diseases / human genetic diseases / Crouzon syndrome / hypotonia / A. FAMILIAL CANCER GENES / severe multiple-joint hypermobility / genetic dwarfism / HEREDITARY EFFECTS OF RADIATION / familial cancer / skeletal disorders / obstructive azoospermia / OF RADIATION-INDUCED CANCERS / meconium ileus / skeletal disorder / chronic sinopulmonary disease / autosomal recessive disease / radiation-induced cancers / /
ANNEX Hereditary effects of radiation CONTENTS Page