Published March, 2013
By Anna Middleton and Jennifer Wiggins
Publisher: Oxford University Press (Oxford University Press Inc)
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This book provides practical advice to assist genetic counselors, geneticists, and other health professionals wanting to engage appropriately with different clients from different communities - patients who are hearing and/or visually impaired, patients with diverse sex development or religious backgrounds, and those who are available only through interpreter or telephone consultation.

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Published March, 2013
By Richard W. Hertle and Louis F. Dell'Osso
Publisher: Oxford University Press (Oxford University Press Inc)
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Availability: Available

This book describes, illustrates, and shares our current understanding, evaluation, and treatments of nystagmus in infancy and childhood. Nystagmus in Infancy and Childhood will provide clinicians with algorithms for examination, descriptions of diagnostic techniques, and medical, surgical, and alternative treatments of the visual system in infants and children with nystagmus.

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Published March, 2013
By Avril Woodhead
Publisher: Springer (Springer-Verlag New York Inc.)
Series: Basic Life Sciences
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Availability: Available

How far can we ignore human variability in risk assessment? The aim of our meeting was to bring together experts from the fields of human epidemiology, toxicology, aging, genetics, carcino genesis and teratology, and to provide a forum in which we might assimi late knowledge of human heterogeneity as a coherent whole.

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Published March, 2013
By Nagy Habib
Publisher: Springer (Springer-Verlag New York Inc.)
Series: Advances in Experimental Medicine and Biology
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Availability: Available

Today we can diagnose abnormalities in ten thousand genes and within a short period of time we will be able to screen through our genome and discover potential abnormalities in our proto-oncogenes, tumour suppressor genes, differentiating genes, apoptotic genes and pro-inflammatory genes.

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Published March, 2013
By David Mittelman
Publisher: Springer (Springer-Verlag New York Inc.)
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Availability: Available

The discovery of stress-induced mutagenesis has changed ideas about mutation and evolution, and revealed mutagenic programs that differ from standard spontaneous mutagenesis in rapidly proliferating cells.

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Published March, 2013
By Ruth F. Chadwick and Alison K. Thompson
Publisher: Springer (Springer-Verlag New York Inc.)
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Availability: Available

Special reference is given in this volume to the implications of genetic information for five different subject areas: eugenics, the insurance industry, the commer cialisation of genetic testing, strategies for raising public awareness, and the value of theo retical ethical and sociological frameworks in the debate.

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Published March, 2013
By Susan Mopper and Sharon Y. Strauss
Publisher: Springer (Springer-Verlag New York Inc.)
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Availability: Available

Providing an essential foundation for evolutionary theory, this comprehensive volume examines patterns of genetic variation within natural insect populations, and explores the underlying mechanisms that lead to the genetic divergence of coexisting organisms.

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Published March, 2013
By Liang Cheng, David Zhang, John N. Eble and David Y. Zhang
Publisher: Springer (Springer-Verlag New York Inc.)
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Availability: Available

Molecular Genetic Pathology, Second Edition presents up-to-date material containing fundamental information relevant to the clinical practice of molecular genetic pathology.

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Published March, 2013
By Robert C. King
Publisher: Springer (Springer-Verlag New York Inc.)
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The purpose of this and future volumes of the Handbook of Genetics is to bring together a collection of relatively short, authoritative essays or annotated compilations of data on topics of~ignificance to geneticists.

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Published March, 2013
By Ulrich Pfeffer
Publisher: Springer
Rating:
Availability: Available

This book offers an overview on the applications of microarray gene expression and copy number variation analyses to the various cancer types. Each chapter addresses a single disease with emphasis on how the genomic analyses have been or can be applied.

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