Lee jun c wong (30 Ergebnisse)

Zustand: New. In English.

Zustand: New.

Hardcover. Zustand: Brand New. 1st edition. 352 pages. 10.00x7.00x0.75 inches. In Stock.

Zustand: New. The variability of clinical symptoms in mitochondrial diseases calls for a systematic presentation of the full range of protocols used in their assessment. This volume provides cutting-edge methods of analysis as well as expert guidance on how to apply them. Editor(s): Wong, Lee-Jun C. Series: Methods in Molecular Biology. Num Pages: 353 pages, 36 black & white tables, biography. BIC Classification: MFN. Category: (P) Professional & Vocational. Dimension: 261 x 184 x 26. Weight in Grams: 838. . 2012. 2012. Hardback. . . . . Books ship from the US and Ireland. …

Zustand: New. In English.

Zustand: New. In English.

Zustand: New. In English.

Zustand: New.

Zustand: Hervorragend. Zustand: Hervorragend | Seiten: 316 | Sprache: Englisch | Produktart: Bücher | In recent years, owing to the fast development of a variety of sequencing technologies in the post human genome project era, sequencing analysis of a group of target genes, entire protein coding regions of the human genome, and the whole human genome has become a reality.  Next Generation Sequencing (NGS) or Massively Parallel Sequencing (MPS) technologies offers a way to screen for mutations in many different genes in a cost and time efficient manner by deep coverage of the target sequences.  This novel technology has now been applied to clinical diagnosis of Mendelian disorders of well characterized or undefined diseases, discovery of new disease genes, noninvasive prenatal diagnosis using maternal blood, and population based carrier testing of severe autosomal recessive disorders.  This book covers topics of these applications, including potential limitations and expanded application in the future.    ¿.…

Taschenbuch. Zustand: Neu. Mitochondrial Disorders | Biochemical and Molecular Analysis | Lee-Jun C. Wong | Taschenbuch | xi | Englisch | 2016 | Humana | EAN 9781493959501 | Verantwortliche Person für die EU: Humana Press in Springer Science + Business Media, Heidelberger Platz 3, 14197 Berlin, juergen[dot]hartmann[at]springer[dot]com | Anbieter: preigu. …

Taschenbuch. Zustand: Neu. Mitochondrial Disorders Caused by Nuclear Genes | Lee-Jun C. Wong | Taschenbuch | xii | Englisch | 2014 | Springer | EAN 9781489992413 | Verantwortliche Person für die EU: Springer Verlag GmbH, Tiergartenstr. 17, 69121 Heidelberg, juergen[dot]hartmann[at]springer[dot]com | Anbieter: preigu.…

Taschenbuch. Zustand: Neu. Next Generation Sequencing Based Clinical Molecular Diagnosis of Human Genetic Disorders | Lee-Jun C. Wong | Taschenbuch | viii | Englisch | 2018 | Springer | EAN 9783319859095 | Verantwortliche Person für die EU: Springer Verlag GmbH, Tiergartenstr. 17, 69121 Heidelberg, juergen[dot]hartmann[at]springer[dot]com | Anbieter: preigu. …

Paperback. Zustand: Brand New. reprint edition. 353 pages. 10.00x7.01x0.86 inches. In Stock.

Zustand: New. 2016. Softcover reprint of the original 1st ed. 2012. paperback. . . . . . Books ship from the US and Ireland.

Zustand: Good. cover leicht beschädigt.

Hardcover. Zustand: Brand New. 1st edition. 369 pages. 9.00x6.00x0.80 inches. In Stock.

Taschenbuch. Zustand: Neu. Druck auf Anfrage Neuware - Printed after ordering - Mitochondrial cytopathies are mutations in the inherited maternal mitochondrial genome, or the nuclear DNA-mutation. Mitochondrial respiratory chain disorders (RCD) are a group of genetically and clinically heterogeneous diseases, due to the fact that protein components of the respiratory chain are encoded by both mitochondrial and nuclear genomes and are essential in all cells. In addition, the biogenesis, structure and function of mitochondria, including DNA replication, transcription, and translation, all require nuclear encoded genes. Since mitochondria are present in every cell, every tissue, mitochondrial disorder usually affects multiple organs.…

Taschenbuch. Zustand: Neu. Druck auf Anfrage Neuware - Printed after ordering - Next Generation Sequencing technology has been applied to clinical diagnoses in the past three to five years using various approaches, including target gene panels and whole exomes. The purpose of this book is to summarize the experiences, the results, advantages and disadvantages, along with future development in the area of NGS-based molecular diagnosis. This up-to-date volume will not only provide the readers working with Next Generation Sequencing the basics on how to apply the technology to molecular diagnosis, but will present the results and experience of practical application.…

Buch. Zustand: Neu. Druck auf Anfrage Neuware - Printed after ordering - Next Generation Sequencing technology has been applied to clinical diagnoses in the past three to five years using various approaches, including target gene panels and whole exomes. The purpose of this book is to summarize the experiences, the results, advantages and disadvantages, along with future development in the area of NGS-based molecular diagnosis. This up-to-date volume will not only provide the readers working with Next Generation Sequencing the basics on how to apply the technology to molecular diagnosis, but will present the results and experience of practical application.…

Zustand: New. In English.

Zustand: New. In English.

HRD. Zustand: New. New Book. Shipped from UK. Established seller since 2000.

HRD. Zustand: New. New Book. Shipped from UK. Established seller since 2000.

Taschenbuch. Zustand: Neu. Next Generation Sequencing | Translation to Clinical Diagnostics | Lee-Jun C. Wong | Taschenbuch | xi | Englisch | 2015 | Springer | EAN 9781489985491 | Verantwortliche Person für die EU: Springer Verlag GmbH, Tiergartenstr. 17, 69121 Heidelberg, juergen[dot]hartmann[at]springer[dot]com | Anbieter: preigu. …

Paperback. Zustand: Brand New. reprint edition. 364 pages. 9.25x6.10x0.85 inches. In Stock.

Zustand: New. Will cover topics of these next generation sequencing applications, including potential limitations and expanded application in the future Readers will learn current technologies, various gene enrichment methods and massively parallel sequencing p.

Zustand: gut. Next Generation Sequencing Based Clinical Molecular Diagnosis of Human Genetic Disorders In deutscher Sprache. pages.

Taschenbuch. Zustand: Neu. Druck auf Anfrage Neuware - Printed after ordering - In recent years, owing to the fast development of a variety of sequencing technologies in the post human genome project era, sequencing analysis of a group of target genes, entire protein coding regions of the human genome, and the whole human genome has become a reality. Next Generation Sequencing (NGS) or Massively Parallel Sequencing (MPS) technologies offers a way to screen for mutations in many different genes in a cost and time efficient manner by deep coverage of the target sequences. This novel technology has now been applied to clinical diagnosis of Mendelian disorders of well characterized or undefined diseases, discovery of new disease genes, noninvasive prenatal diagnosis using maternal blood, and population based carrier testing of severe autosomal recessive disorders. This book covers topics of these applications, including potential limitations and expanded application in the future.…

Buch. Zustand: Neu. Druck auf Anfrage Neuware - Printed after ordering - In recent years, owing to the fast development of a variety of sequencing technologies in the post human genome project era, sequencing analysis of a group of target genes, entire protein coding regions of the human genome, and the whole human genome has become a reality. Next Generation Sequencing (NGS) or Massively Parallel Sequencing (MPS) technologies offers a way to screen for mutations in many different genes in a cost and time efficient manner by deep coverage of the target sequences. This novel technology has now been applied to clinical diagnosis of Mendelian disorders of well characterized or undefined diseases, discovery of new disease genes, noninvasive prenatal diagnosis using maternal blood, and population based carrier testing of severe autosomal recessive disorders. This book covers topics of these applications, including potential limitations and expanded application in the future.…

Zustand: Gut. Gebundene Ausgabe Insgesamt gutes, ordentliches Exemplar. Lediglich leichte Spuren der Zeit am Einband. Sprache: Deutsch Gewicht in Gramm: 550.