Nuclear Family

Merosin-positive congenital muscular dystrophy with transient brain dysmyelination, pontocerebellar hypoplasia and mental retardation

Genetics / Pathology / Cognitive Science / Skeletal muscle biology / Magnetic Resonance Imaging / Epilepsy / Histology / Immunohistochemistry / Creatine / Magnetic Resonance Spectroscopy / Adolescent / Intellectual Disability / Brain development / Israel / Biopsy / Mental Retardation / London / Brain / Humans / Child / Cerebellum / Muscle / Cerebral Cortex / Haplotypes / Microcephaly / Female / Muscular Dystrophies / Male / Muscles / Infant / Developmental disabilities / Cataract / D-Aspartic Acid / Medical Physiology / Pedigree / Creatine Kinase / Genetic linkage analysis / Clinical Sciences / Spectrum / Fluorescent Antibody Technique / Family Health / Facies / Adult / Neuromuscular Disorders / Time Factors / Consanguinity / Nuclear Family / Neuronal Migration / Neuropediatrics / Dystrophin / X ray Computed Tomography / Choline / Nuclear Magnetic Resonance Imaging / Genetic Markers / Neurosciences / Linkage Analysis / Nino / Myelin Sheath / Magnetic resonance image / Laminin / Congenital muscular dystrophy / Child preschool / Epilepsy / Histology / Immunohistochemistry / Creatine / Magnetic Resonance Spectroscopy / Adolescent / Intellectual Disability / Brain development / Israel / Biopsy / Mental Retardation / London / Brain / Humans / Child / Cerebellum / Muscle / Cerebral Cortex / Haplotypes / Microcephaly / Female / Muscular Dystrophies / Male / Muscles / Infant / Developmental disabilities / Cataract / D-Aspartic Acid / Medical Physiology / Pedigree / Creatine Kinase / Genetic linkage analysis / Clinical Sciences / Spectrum / Fluorescent Antibody Technique / Family Health / Facies / Adult / Neuromuscular Disorders / Time Factors / Consanguinity / Nuclear Family / Neuronal Migration / Neuropediatrics / Dystrophin / X ray Computed Tomography / Choline / Nuclear Magnetic Resonance Imaging / Genetic Markers / Neurosciences / Linkage Analysis / Nino / Myelin Sheath / Magnetic resonance image / Laminin / Congenital muscular dystrophy / Child preschool

Preferential Transmission of Paternal Alleles at Risk Genes in Attention-Deficit/Hyperactivity Disorder

Genetics / Attention-Deficit/Hyperactivity Disorder / Ireland / Molecular Psychiatry / Biological Sciences / Humans / Female / Male / Animal Model / Odds ratio / Nuclear Family / Linkage Disequilibrium / Chi Square Distribution / Genetic Association / Genetic Markers / The American / Humans / Female / Male / Animal Model / Odds ratio / Nuclear Family / Linkage Disequilibrium / Chi Square Distribution / Genetic Association / Genetic Markers / The American

New familial mitochondrial encephalopathy with macrocephaly, cardiomyopathy, and complex I deficiency

Skeletal muscle biology / Humans / Male / Infant / Phenotype / Clinical Sciences / Head / Family Health / Myocardium / Nuclear Family / Cardiomyopathies / Two-Dimensional Gel Electrophoresis / Human Fibroblasts / Lactic Acid / Neurosciences / Clinical Sciences / Head / Family Health / Myocardium / Nuclear Family / Cardiomyopathies / Two-Dimensional Gel Electrophoresis / Human Fibroblasts / Lactic Acid / Neurosciences

Unilateral lobar pulmonary agenesis in sibs

Medical Genetics / Biological Sciences / Humans / Female / Male / Lung / Adult / Nuclear Family / Lung / Adult / Nuclear Family

New familial mitochondrial encephalopathy with macrocephaly, cardiomyopathy, and complex I deficiency

Skeletal muscle biology / Humans / Male / Infant / Phenotype / Clinical Sciences / Head / Family Health / Myocardium / Nuclear Family / Cardiomyopathies / Two-Dimensional Gel Electrophoresis / Human Fibroblasts / Two dimensional Gel Electrophoresis / Lactic Acid / Neurosciences / Clinical Sciences / Head / Family Health / Myocardium / Nuclear Family / Cardiomyopathies / Two-Dimensional Gel Electrophoresis / Human Fibroblasts / Two dimensional Gel Electrophoresis / Lactic Acid / Neurosciences

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