Edité par Academic Press 29.09.2015., 2015
ISBN 10 : 0128017392 ISBN 13 : 9780128017395
Langue: anglais
Vendeur : ABC Versand e.K., Aarbergen, Allemagne
EUR 14,26
Autre deviseQuantité disponible : 1 disponible(s)
Ajouter au panierEtat : Gut. Auflage: Illustrated. 334 Seiten kleine Gebrauchsspuren, innen sauber und ordentlich. kleiner Fleck auf dem unteren Buchschnitt Q53 Sprache: Englisch Gewicht in Gramm: 756 19,1 x 1,9 x 23,5 cm, Taschenbuch.
Edité par Academic Press 2015-10-01, 2015
ISBN 10 : 0128017392 ISBN 13 : 9780128017395
Langue: anglais
Vendeur : Chiron Media, Wallingford, Royaume-Uni
EUR 75,01
Autre deviseQuantité disponible : Plus de 20 disponibles
Ajouter au panierPaperback. Etat : New.
Edité par Elsevier Science Publishing Co Inc, 2015
ISBN 10 : 0128017392 ISBN 13 : 9780128017395
Langue: anglais
Vendeur : THE SAINT BOOKSTORE, Southport, Royaume-Uni
EUR 95,37
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Ajouter au panierPaperback / softback. Etat : New. New copy - Usually dispatched within 4 working days. 846.
Vendeur : Revaluation Books, Exeter, Royaume-Uni
EUR 85,41
Autre deviseQuantité disponible : 2 disponible(s)
Ajouter au panierPaperback. Etat : Brand New. 208 pages. 9.00x7.50x0.75 inches. In Stock.
Vendeur : Mispah books, Redhill, SURRE, Royaume-Uni
EUR 128,38
Autre deviseQuantité disponible : 1 disponible(s)
Ajouter au panierPaperback. Etat : Like New. Like New. book.
Vendeur : Brook Bookstore On Demand, Napoli, NA, Italie
EUR 81,31
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Ajouter au panierEtat : new. Questo è un articolo print on demand.
Edité par Elsevier Science Sep 2015, 2015
ISBN 10 : 0128017392 ISBN 13 : 9780128017395
Langue: anglais
Vendeur : BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, Allemagne
EUR 87,95
Autre deviseQuantité disponible : 2 disponible(s)
Ajouter au panierTaschenbuch. Etat : Neu. This item is printed on demand - it takes 3-4 days longer - Neuware - Clinical Applications for Next Generation Sequencing provides readers with an outstanding postgraduate resource to learn about the translational use of NGS in clinical environments. Rooted in both medical genetics and clinical medicine, the book fills the gap between state-of-the-art technology and evidence-based practice, providing an educational opportunity for users to advance patient care by transferring NGS to the needs of real-world patients. The book builds an interface between genetic laboratory staff and clinical health workers to not only improve communication, but also strengthen cooperation. Users will find valuable tactics they can use to build a systematic framework for understanding the role of NGS testing in both common and rare diseases and conditions, from prenatal care, like chromosomal abnormalities, up to advanced age problems like dementia. 334 pp. Englisch.
Edité par Elsevier Science & Technology|Academic Press, 2015
ISBN 10 : 0128017392 ISBN 13 : 9780128017395
Langue: anglais
Vendeur : moluna, Greven, Allemagne
EUR 89,02
Autre deviseQuantité disponible : Plus de 20 disponibles
Ajouter au panierEtat : New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Clinical Applications for Next Generation Sequencing provides readers with an outstanding postgraduate resource to learn about the translational use of NGS in clinical environments. Rooted in both medical genetics and clinical med.
Vendeur : AHA-BUCH GmbH, Einbeck, Allemagne
EUR 99,65
Autre deviseQuantité disponible : 2 disponible(s)
Ajouter au panierTaschenbuch. Etat : Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Clinical Applications for Next Generation Sequencing provides readers with an outstanding postgraduate resource to learn about the translational use of NGS in clinical environments. Rooted in both medical genetics and clinical medicine, the book fills the gap between state-of-the-art technology and evidence-based practice, providing an educational opportunity for users to advance patient care by transferring NGS to the needs of real-world patients. The book builds an interface between genetic laboratory staff and clinical health workers to not only improve communication, but also strengthen cooperation. Users will find valuable tactics they can use to build a systematic framework for understanding the role of NGS testing in both common and rare diseases and conditions, from prenatal care, like chromosomal abnormalities, up to advanced age problems like dementia.