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Textbook of Human Reproductive Genetics [Mīkstie vāki]

Edited by (Vrije Universiteit Brussel), Edited by
  • Formāts: Paperback / softback, 200 pages, height x width x depth: 244x187x10 mm, weight: 500 g, 13 Tables, black and white; 19 Plates, color; 11 Halftones, unspecified; 34 Line drawings, unspecified
  • Izdošanas datums: 10-Apr-2014
  • Izdevniecība: Cambridge University Press
  • ISBN-10: 1107683580
  • ISBN-13: 9781107683587
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  • Cena: 66,41 €
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  • Formāts: Paperback / softback, 200 pages, height x width x depth: 244x187x10 mm, weight: 500 g, 13 Tables, black and white; 19 Plates, color; 11 Halftones, unspecified; 34 Line drawings, unspecified
  • Izdošanas datums: 10-Apr-2014
  • Izdevniecība: Cambridge University Press
  • ISBN-10: 1107683580
  • ISBN-13: 9781107683587
Citas grāmatas par šo tēmu:
What happens with our genome and epigenome in the first fundamental days of our development? How can this be analysed? What do we need to know when faced with patients' questions about their own infertility, or how to prevent the birth of affected children? For the first time, this book brings together both scientists' and clinicians' viewpoints on human reproductive genetics, making for a more comprehensive discussion of interest to ART professionals and developmental biologists. With worldwide leaders in this burgeoning field guiding the reader through from the basics to the most exciting recent discoveries, this book presents the wider picture of how reproductive medicine and biology links with genetics. The editors also address the new challenges raised in how to treat and counsel patients at fertility and genetic clinics, as well as eliciting vivid bioethical debates. This book brings together genetics, reproductive biology and medicine for practitioners and geneticists.

Papildus informācija

This book brings together genetics, reproductive biology and medicine for an integrative view of the emerging specialism of reproductive genetics.
List of contributors
vii
Preface ix
1 Basic genetics and cytogenetics: a brief reminder
1(14)
Karen Sermon
2 How to analyze a single blastomere? Application of whole genome technologies: microarrays and next generation sequencing
15(18)
Parveen Kumar
Masoud Zamani Esteki
Niels Van der Aa
Thierry Voet
3 Meiosis: how to get a good start in life
33(19)
Ursula Eichenlaub-Ritter
4 Chromosomes in early human embryo development: incidence of chromosomal abnormalities, underlying mechanisms and consequences for development
52(16)
Esther B. Baart
Diane Van Opstal
5 DNA is not the whole story: transgenerational epigenesis and imprinting
68(15)
Ashwini Balakrishnan
J. Richard Chaillet
6 Genes are not the whole story: retrotransposons as new determinants of male fertility
83(14)
Patricia Fauque
Deborah Bourc'his
7 Chromosomal causes of infertility: the story continues
97(16)
Svetlana A. Yatsenko
Aleksandar Rajkovic
8 Genes and infertility
113(14)
Inge Liebaers
Elias El Inati
Willy Lissens
Stephane Viville
9 Genetic counseling and gamete donation in assisted reproductive treatment
127(19)
Alison Lashwood
Alison Bagshawe
10 Genetic testing for infertile patients
146(11)
Willem Verpoest
11 Preimplantation genetic diagnosis
157(15)
Jan Traeger-Synodinos
Catherine Staessen
12 Epigenetics and assisted reproductive technology
172(12)
Aafke P. A. van Montfoort
13 Ethical considerations in human reproductive genetics
184(15)
Guido de Wert
Wybo Dondorp
Index 199
Karen Sermon is Professor, Research Group Reproduction and Genetics, Vrije Universiteit Brussel, Brussels, Belgium. Stéphane Viville is Professor in the Institute de Génétique et de Biologie Moléculaire, University of Strasbourg, Strasbourg, France.