Search Results - Genetic Variation.

Evolving genomic approaches to the study of complex cardiovascular diseases in human populations genetic and genomic epidemiology /

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Evolving genomic approaches to the study of complex cardiovascular diseases in human populations genetic and genomic epidemiology /

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Bioinformatics tools in conservation biology

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Bioinformatics tools in conservation biology

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Array comparative genomic hybridisation to characterise copy number variation in the human genome

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Quantitative CNV testing in molecular diagnostics

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Human migration and population structure part 1 of 2 /

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Neurogenetic developmental disorders variation of manifestation in childhood /

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Racial and ethnic variation in systemic lupus erythematosus and systemic sclerosis (Scleroderma)

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Racial and ethnic variation in systemic lupus erythematosus and systemic sclerosis (Scleroderma)

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The impact of genomic architecture and diversity on infectious diseases

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Analysis of protein-protein interaction, transcriptional regulation and metabolic networks

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Specimen banking saving for the future /

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Specimen banking saving for the future /

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Evolution in four dimensions : genetic, epigenetic, behavioral, and symbolic variation in the history of life / by Jablonka, Eva, Lamb, Marion J.

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Ancient DNA and human evolutionary inference

Table of Contents: “…Contents: Patterns of genetic variation in Europe and the Neolithic -- Ancient DNA and anatomically modern humans (Challenges & Potential) -- The Neolithic transition in Europe (Scandinavia, Iberia and Eastern Europe).…”
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The case for offering all women amniocentesis and chromosomal microarray analysis

Table of Contents: “…Contents: Array-based copy number analysis (ABCNA) -- Chromosomal microarray analysis (CMA) -- CMA methodology -- Targeted patient population -- Detection of clinically significant abnormalities -- Copy number variation -- CMA vs. karyotype -- Prenatal use of arrays -- Microarray genetic screening -- Search and destroy concern and eugenics -- Tests which should be abandoned -- Prenatal CMA clinical protocol -- Array-CGH -- Findings of uncertain significance -- Recent cases -- Interpreting uncertain array data -- Advantages of amino and array analysis -- Two kinds of uncertainty -- Non-paternity concerns -- Study design.…”
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Developmental plasticity the 3rd dimension of phenotypic variation and disease risk /

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Developmental plasticity the 3rd dimension of phenotypic variation and disease risk /

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Mendelian CNV mutations

Table of Contents: “…Contents: Copy number variation has now been shown to be a major cause of human genetic variation -- It has been implicated as the main cause of mental retardation disorders -- The boundary between benign and malignant copy number variations is blurring -- This is because certain CNVs can be benign but cause genetic disorders dependent on copy number state, sex and genetic background -- We coin them "Mendelian CNVs" -- An overview of autosomal recessive, dominant, X-linked and imprinted CNVs -- Diagnostic and clinical consequences.…”
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