Search Results - "Genetics"

Factor VIII and Haemophilia A

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Mapping our genes : the Genome Project and the future of medicine / by Wingerson, Lois

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Language, Meaning, Interpretation by Fløistad, Guttorm

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Knowledge and reality Essays in Honor of Alvin Plantinga / by Crisp, Thomas M.

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Knowing Art Essays in Aesthetics and Epistemology / by Kieran, Matthew

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Kant's Critique of Pure Reason The Foundation of Modern Philosophy / by Hffe, Otfried

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Ethics and biotechnology

Subjects: An electronic book accessible through the World Wide Web; click to view

Oncogenomics molecular approaches to cancer /

Subjects: “…Cancer Genetic aspects.…”
An electronic book accessible through the World Wide Web; click to view

Nutrigenomics and beyond informing the future : workshop summary /

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Neurogenetic developmental disorders variation of manifestation in childhood /

Subjects: “…Developmental disabilities Genetic aspects.…”
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Gene sharing and evolution the diversity of protein functions / by Piatigorsky, Joram

Subjects: “…Genetic regulation.…”
An electronic book accessible through the World Wide Web; click to view

Evolution of virulence in eukaryotic microbes

Table of Contents: “…General overviews -- pt. 2. Population genetics and evolutionary approaches -- pt. 3. Forward and reverse genetic systems for defining virulence -- pt. 4. …”
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Transgenic plants recent developments /

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Origins of intelligence the evolution of cognitive development in monkeys, apes, and humans / by Parker, Sue Taylor

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Post-autism : a psychoanalytical narrative, with supervisions by Donald Meltzer / by Mélega, Marisa Pelella

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The atomized body : the cultural life of stem cells, genes and neurons /

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The genealogy of a gene : patents, HIV/AIDS, and race / by Jackson, Myles W.

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Genomic disorders mechanisms for copy number variation (CNV) and clinical implementation of high-resolution genome analysis /

Table of Contents: “…Contents: Rearrangements of the human genome as a significant source for genetic variation -- Genomic disorders -- Inherited and sporadic traits -- Rearrangements associated with genomic disorders can be recurrent, with breakpoint clusters resulting in a common sized deletion/duplication, or nonrecurrent and of different sizes -- Nonallelic homologous recombination (NAHR) -- Nonhomologous end-joining (NHEJ) -- Low-copy repeats (LCRs) -- Fork Stalling and Template Switching (FoSTeS) -- Rearrangements as an evolutionary function -- Gene dosage, position effects, unmasking of coding region mutations (cSNPs) and other functional SNPs -- De novo genomic rearrangements have been shown to cause both chromosomal and Mendelian disease, as well as sporadic traits -- Understanding of the extent to which genomic rearrangements, gene CNV, and/or gene dosage alterations are responsible for common and complex traits remains rudimentary.…”
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Copy number variation in mental retardation

Table of Contents: “…Contents: Genetics of mental retardation -- Microarray-based detection of copy number variation (CNV) -- CNVs in mental retardation, a frequent cause -- Molecular karyotyping, improving diagnostic yield.…”
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Copy number variation in neuropsychiatric disorders

Table of Contents: “…Contents: Copy Number Variation (CNV) in the human genome -- General characteristics -- Detection methodologies -- Copy number variation and human disease -- Cataloguing and assessing the biological impact of a copy number variant -- The genetic basis of Autism spectrum disorder (ASD) and the role of CNVs in ASD etiology -- Variable neuropsychiatric phenotypes associated with copy number variation -- Diagnostic and interpretation challenges.…”
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