Molecular Genetics - Page 2

Racial Differences in Genetic and Environmental Risk to Preterm Birth

Genetics / Molecular Genetics / Multidisciplinary / Twins / Social Inequality / Environmental Risk / Pregnancy / Humans / African American / Female / Male / Siblings / PLoS one / Analysis of Variance / Gestational Age / Preterm Birth / Environmental Exposure / Premature Birth / Racial differences / Environmental Risk / Pregnancy / Humans / African American / Female / Male / Siblings / PLoS one / Analysis of Variance / Gestational Age / Preterm Birth / Environmental Exposure / Premature Birth / Racial differences

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Laboratory practical work as a technological process

Problem Based Learning / Molecular Genetics / Enzyme Kinetics / Biochemical / Model System / Curriculum and Pedagogy / Biochemical education / Curriculum and Pedagogy / Biochemical education

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Laboratory practical work as a technological process

Problem Based Learning / Molecular Genetics / Enzyme Kinetics / Biochemical / Model System / Curriculum and Pedagogy / Biochemical education / Curriculum and Pedagogy / Biochemical education

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Síndrome de Andersen-Tawil: una revisión del diagnóstico genético y clínico con énfasis en sus manifestaciones cardíacas

Genetics / Genomics / Molecular Genetics / Humans / Pedigree / Clinical Sciences / Massive Sequencing and Microarray Pdf / Heart Diseases / Clinical Sciences / Massive Sequencing and Microarray Pdf / Heart Diseases

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Does a peculiar EEG pattern exist also for FRAXE mental retardation?

Engineering / Genetics / Electroencephalography / Obsessive-Compulsive Disorder / Molecular Genetics / Intellectual Disability / Mental Retardation / Brain Mapping / Brain / Humans / Child / Clinical / Male / Reading and writing / Proteins / Clinical Neurophysiology / Somatosensory Evoked Potentials / Developmental delay / Median Nerve / Intellectual Disability / Mental Retardation / Brain Mapping / Brain / Humans / Child / Clinical / Male / Reading and writing / Proteins / Clinical Neurophysiology / Somatosensory Evoked Potentials / Developmental delay / Median Nerve

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Genetic characterization of Fasciola hepatica from Tunisia and Algeria based on mitochondrial and nuclear DNA sequences

Genetics / Microbiology / Parasitology / Medical Microbiology / Molecular Genetics / Molecular Epidemiology / Phylogeny / Mitochondrial DNA / Algeria / Tunisia / Tropics / North Africa / Sheep / Parasite / Animals / Fasciola hepatica / Cluster Analysis / Cytochrome c oxidase / nuclear DNA / Cattle / Molecular Characterization / SHEEP DISEASES / Veterinary Sciences / Ribosomal DNA / Ribosomes / Helminths / Mitochondrial Proteins / Molecular Epidemiology / Phylogeny / Mitochondrial DNA / Algeria / Tunisia / Tropics / North Africa / Sheep / Parasite / Animals / Fasciola hepatica / Cluster Analysis / Cytochrome c oxidase / nuclear DNA / Cattle / Molecular Characterization / SHEEP DISEASES / Veterinary Sciences / Ribosomal DNA / Ribosomes / Helminths / Mitochondrial Proteins

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Glutaric aciduria type 1 in South Africa—high incidence of glutaryl-CoA dehydrogenase deficiency in black South Africans

Molecular Genetics / South Africa / Humans / Female / Male / Infant / Incidence / Newborn Screening / Clinical Sciences / South African / Newborn Infant / Organic Acid / Infant / Incidence / Newborn Screening / Clinical Sciences / South African / Newborn Infant / Organic Acid

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Preimplantation genetic diagnosis for mitochondrial DNA disorders: ethical guidance for clinical practice

Genetics / Ethics / Human Genetics / Informed Consent / Molecular Genetics / Genetic counseling / Cytogenetics / Clinical Practice / Pregnancy / Mitochondrial DNA / Humans / Genetic Testing / Mutation / Female / Feasibility Studies / Clinical Genetics / Preimplantation genetic diagnosis / Embryo Research / Mitochondrial Diseases / Scientific Research / Minor / Health risk / Embryos / Clinical Application / Good Clinical Practice in Clinical Trials / Genetic counseling / Cytogenetics / Clinical Practice / Pregnancy / Mitochondrial DNA / Humans / Genetic Testing / Mutation / Female / Feasibility Studies / Clinical Genetics / Preimplantation genetic diagnosis / Embryo Research / Mitochondrial Diseases / Scientific Research / Minor / Health risk / Embryos / Clinical Application / Good Clinical Practice in Clinical Trials

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Atypical expression of cleidocranial dysplasia: clinical and molecular-genetic analysis

Dentistry / Molecular Genetics / Adolescent / Transcription Factors / Cephalometry / Humans / Male / Differential Diagnosis / Facies / Craniofacial Orthodontics / Rubinstein-Taybi syndrome / Humans / Male / Differential Diagnosis / Facies / Craniofacial Orthodontics / Rubinstein-Taybi syndrome

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Genetic variation studies in Oryctes rhinoceros (L.) (Coleoptera: Scarabaeidae) using single locus DNA microsatellite markers

Pest Management / Southeast Asia / Population genetics (Biology) / Agricultural Entomology / Molecular Genetics / Palm Oil Plantation / Oil palm / Beetles / Insect pheromones / Microsatellite DNA / Palm Oil Plantation / Oil palm / Beetles / Insect pheromones / Microsatellite DNA

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Consideraciones diagnósticas sobre el Síndrome MELAS

Genetics / Electroencephalography / Molecular Genetics / Cerebrospinal Fluid / Mitochondrial DNA / Case Report / Lactic Acid / Case Report / Lactic Acid

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Secondary creatine deficiency in ornithine delta-aminotransferase deficiency

Magnetic Resonance Imaging / Epilepsy / Creatine / Molecular Genetics / Magnetic Resonance Spectroscopy / Adolescent / Intellectual Disability / Brain / Humans / Child / Aggression / Female / Male / Young Adult / Clinical Sciences / Adult / Retrospective Studies / Adolescent / Intellectual Disability / Brain / Humans / Child / Aggression / Female / Male / Young Adult / Clinical Sciences / Adult / Retrospective Studies

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TOXIC HYDROGEN SULFIDE AND DARK CAVES: PHENOTYPIC AND GENETIC DIVERGENCE ACROSS TWO ABIOTIC ENVIRONMENTAL GRADIENTS IN POECILIA MEXICANA

Evolutionary Biology / Geography / Gene Flow / Population Genetics / Evolution / Quantitative Genetics / Molecular Genetics / Developmental Plasticity / Ecological Speciation / Female / Animals / Male / Spatial Scale / Biological evolution / Phenotype / Environmental Gradient / Divergent Selection / Poecilia / Genetic Differentiation / Reproductive Isolation / Local adaptation / Environmental Conditions / Gills / Hydrogen Sulfide / Genetic Divergence / Cytochrome B Gene / Phenotypic variation / Environment / Genetic Markers / Environmental Exposure / Extremophile / Quantitative Genetics / Molecular Genetics / Developmental Plasticity / Ecological Speciation / Female / Animals / Male / Spatial Scale / Biological evolution / Phenotype / Environmental Gradient / Divergent Selection / Poecilia / Genetic Differentiation / Reproductive Isolation / Local adaptation / Environmental Conditions / Gills / Hydrogen Sulfide / Genetic Divergence / Cytochrome B Gene / Phenotypic variation / Environment / Genetic Markers / Environmental Exposure / Extremophile

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Síndrome de Andersen-Tawil: una revisión del diagnóstico genético y clínico con énfasis en sus manifestaciones cardíacas

Genetics / Genomics / Molecular Genetics / Humans / Pedigree / Clinical Sciences / Massive Sequencing and Microarray Pdf / Heart Diseases / Clinical Sciences / Massive Sequencing and Microarray Pdf / Heart Diseases

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Glutaric aciduria type 1 in South Africa-high incidence of glutaryl-CoA dehydrogenase deficiency in black South Africans

Molecular Genetics / South Africa / Humans / Female / Male / Infant / Incidence / Newborn Screening / Clinical Sciences / South African / Newborn Infant / Organic Acid / Infant / Incidence / Newborn Screening / Clinical Sciences / South African / Newborn Infant / Organic Acid

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Phenylalanine hydroxylase deficiency: Molecular epidemiology and predictable BH4-responsiveness in South Portugal PKU patients

Polymorphism / Molecular Genetics / Molecular Epidemiology / Portugal / Humans / Haplotypes / Phenylketonuria / Genetic Association Studies / Phenotype / Clinical Sciences / Spectrum / Genomic DNA / Molecular Characterization / Phenylalanine hydroxylase / Haplotypes / Phenylketonuria / Genetic Association Studies / Phenotype / Clinical Sciences / Spectrum / Genomic DNA / Molecular Characterization / Phenylalanine hydroxylase

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