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Liehr Thomas (181 results)
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Condition: very good. Gut/Very good: Buch bzw. Schutzumschlag mit wenigen Gebrauchsspuren an Einband, Schutzumschlag oder Seiten. / Describes a book or dust jacket that does show some signs of wear on either the binding, dust jacket or pages.
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Schutz der Minderheiten - in: Betriebsverfassungsgesetz - Aus der Ersten, Zweiten und Dritten Beratung des Deutschen Bundestages. Zur Sache 01/72.
Language: German
Published by Presse- u. Informationszentrum d. Dt. Bundestages;, 1971
Seller: books4less (Versandantiquariat Petra Gros GmbH & Co. KG), Welling, Germany
Seller rating 5 out of 5 stars
Broschiert. Condition: Gut. 271 Seiten; Der Erhaltungszustand des hier angebotenen Werks ist trotz seiner Bibliotheksnutzung sehr sauber und kann entsprechende Merkmale aufweisen (Rückenschild, Instituts-Stempel.). Neben dem oben aufgeführten Aufsatz befinden sich auch weitere Beiträge auch anderer Autoren in dem Werk. Sprache: Deutsch Gewicht in Gramm: 310.
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Taschenbuch. Condition: Neu. Druck auf Anfrage Neuware - Printed after ordering - This book is a general overview on Human Genetics including:- an attempt for a definition and a short history of Human Genetics;- Mendel's rules, basics on mitosis, meiosis and mutations;- an overview on clinical genetics including, pedigrees, modes of inheritance and genetic counseling;- basics of cytogenetics, molecular cytogenetics and molecular genetics;- pre- and postnatal genetic diagnostics with genomic disorders; and- tumor genetics (including cancer and familial cancer syndromes).- Also aspects of mutagenesis, teratology, gene therapy, population genetics and epigenetics are discussed.Overall, this book is meant as a kind of 'starter package' for interested future human genetics specialists.
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Taschenbuch. Condition: Neu. Druck auf Anfrage Neuware - Printed after ordering - This book is a general overview on Human Genetics including:- an attempt for a definition and a short history of Human Genetics;- Mendel's rules, basics on mitosis, meiosis and mutations;- an overview on clinical genetics including, pedigrees, modes of inheritance and genetic counseling;- basics of cytogenetics, molecular cytogenetics and molecular genetics;- pre- and postnatal genetic diagnostics with genomic disorders; and- tumor genetics (including cancer and familial cancer syndromes).- Also aspects of mutagenesis, teratology, gene therapy, population genetics and epigenetics are discussed.Overall, this book is meant as a kind of 'starter package' for interested future human genetics specialists.
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Taschenbuch. Condition: Neu. Druck auf Anfrage Neuware - Printed after ordering.
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Taschenbuch. Condition: Neu. Human Genetics | A Basic Training Package | Thomas Liehr | Taschenbuch | Englisch | epubli | EAN 9783746797465 | Verantwortliche Person für die EU: preigu GmbH & Co. KG, Lengericher Landstr. 19, 49078 Osnabrück, mail[at]preigu[dot]de | Anbieter: preigu.
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Taschenbuch. Condition: Neu. Human Genetics | A Basic Training Package Edition 2020 | Thomas Liehr | Taschenbuch | 168 S. | Englisch | 2020 | epubli | EAN 9783750276123 | Verantwortliche Person für die EU: Neopubli GmbH, Sebastian Stude, Köpenicker Str. 154a, 10997 Berlin, produktsicherheit[at]epubli[dot]com | Anbieter: preigu.
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Benign and Pathological Chromosomal Imbalances: Microscopic and Submicroscopic Copy Number Variations (CNVs) in Genetics and Counseling
Language: English
Published by Academic Press Inc 2013-11-12, 2013
ISBN 10: 0124046312 ISBN 13: 9780124046313
£ 59.37
£ 15.49 shipping
Ships from United Kingdom to U.S.A.Quantity: Over 20 available
Add to basketHardcover. Condition: New.
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Condition: New. pp. 220.
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Taschenbuch. Condition: Neu. Small supernumerary marker chromosomes | Basics | Dr. Thomas Liehr | Taschenbuch | Englisch | epubli | EAN 9783758451935 | Verantwortliche Person für die EU: preigu GmbH & Co. KG, Lengericher Landstr. 19, 49078 Osnabrück, mail[at]preigu[dot]de | Anbieter: preigu.
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Taschenbuch. Condition: Neu. Druck auf Anfrage Neuware - Printed after ordering - This book is aimed at anyone interested in the biological phenomenon of uniparental disomy (UPD). Since UPD can lead to congenital diseases, this is also an important topic of the book - eight testimonials from affected families are also included.The book answers the following and other questions: - What is a UPD - What is the difference between congenital and acquired UPD - How common is the UPD phenomenon - How can UPD develop - What forms and subtypes of UPD are there - What are the clinical consequences of UPD - Is UPD hereditary - How can UPD be diagnosed - What patient organizations are there - What is imprinting and why can it be connected with UPD - What are imprinting syndromes there - Which research approaches are there - Will there soon be a gene therapy for UPD UPD has long been misunderstood as a molecular genetic problem - here it is put in its proper place as a chromosomal / chromosomic phenomenon. The book is also basis for the correct interpretation of UPD findings from molecular genetics (SNP-array-CGH or NGS).
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Hardcover. Condition: Brand New. 1st edition. 220 pages. 9.00x6.25x0.75 inches. In Stock.
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Condition: New. pp. 220 Index 1st Edition.
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Taschenbuch. Condition: Neu. All you need to know about uniparental disomy | UPD and imprinting. DE | Dr. Thomas Liehr | Taschenbuch | Englisch | epubli | EAN 9783758465581 | Verantwortliche Person für die EU: preigu GmbH & Co. KG, Lengericher Landstr. 19, 49078 Osnabrück, mail[at]preigu[dot]de | Anbieter: preigu.
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Small Supernumerary Marker Chromosomes (sSMC): A Guide for Human Geneticists and Clinicians
Seller: Ria Christie Collections, Uxbridge, United Kingdom
Seller rating 5 out of 5 stars
£ 76.40
£ 11.98 shipping
Ships from United Kingdom to U.S.A.Quantity: Over 20 available
Add to basketCondition: New. In.
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Condition: New. pp. xx + 220 Index.
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Paperback. Condition: New.
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Condition: New. pp. 220.
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Benign and Pathological Chromosomal Imbalances: Microscopic and Submicroscopic Copy Number Variations (CNVs) in Genetics and Counseling
Language: English
Published by Elsevier Science Publishing Co Inc, 2013
ISBN 10: 0124046312 ISBN 13: 9780124046313
Seller: THE SAINT BOOKSTORE, Southport, United Kingdom
Seller rating 5 out of 5 stars
£ 75.26
£ 16.27 shipping
Ships from United Kingdom to U.S.A.Quantity: Over 20 available
Add to basketHardback. Condition: New. New copy - Usually dispatched within 4 working days.
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Human Ring Chromosomes: A Practical Guide for Clinicians and Families
Seller: Books From California, Simi Valley, CA, U.S.A.
Seller rating 4 out of 5 stars
hardcover. Condition: Very Good.
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Human Ring Chromosomes: A Practical Guide for Clinicians and Families
Seller: Books From California, Simi Valley, CA, U.S.A.
Seller rating 4 out of 5 stars
hardcover. Condition: Good. Cover and edges may have some wear.
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Uniparental Disomy (UPD) in Clinical Genetics: A Guide for Clinicians and Patients
Seller: Ria Christie Collections, Uxbridge, United Kingdom
Seller rating 5 out of 5 stars
£ 86.64
£ 11.98 shipping
Ships from United Kingdom to U.S.A.Quantity: Over 20 available
Add to basketCondition: New. In.
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Uniparental Disomy in Clinical Genetics : A Guide for Clinicians and Patients
Seller: GreatBookPricesUK, Woodford Green, United Kingdom
Seller rating 5 out of 5 stars
Condition: New.
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Small Supernumerary Marker Chromosomes (sSMC): A Guide for Human Geneticists and Clinicians
Seller: Ria Christie Collections, Uxbridge, United Kingdom
Seller rating 5 out of 5 stars
£ 96.88
£ 11.98 shipping
Ships from United Kingdom to U.S.A.Quantity: Over 20 available
Add to basketCondition: New. In.
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Condition: New. pp. 192.
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Paperback. Condition: Brand New. 2012 edition. 250 pages. 9.26x6.11x0.70 inches. In Stock.
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Human Ring Chromosomes (Hardcover)
Language: English
Published by Springer International Publishing AG, Cham, 2024
ISBN 10: 3031475291 ISBN 13: 9783031475290
Hardcover. Condition: new. Hardcover. This book presents chromosome-wise clinical cases following an evidence-based protocol, in addition to providing the scientific background on the mechanisms of human ring chromosome (RC) formation. Presence of RCs in a genome can lead to several rare genetic diseases. This book, edited by the leading experts Prof. Peining Li and Prof. Thomas Liehr, is the first comprehensive book on this topic.Over the past 60 years, banding cytogenetics, fluorescence in situ hybridization, chromosome microarray analysis, and whole genome sequencing have been used to diagnose cases with a RC. Ring syndrome of sever growth retardation and variable intellectual disability has been considered a common clinical feature for all RCs. Clinical heterogeneity of chromosome-specific deletion and duplication syndromes, gene-related organ and tissue defects, cancer predisposition to different types of tumors, and reproduction failure has been reported in the literature. However, the cases of RCs reportedin the literature account for less than 1% of its real occurrence. Current diagnostic practice lacks laboratory standards for analyzing cellular behavior and genomic imbalances of RCs to evaluate its compound effects on patients. The under-representation of clinical cases and the lack of comprehensive diagnostic analysis make challenging to establish accurate clinico-cytogenomic correlations. Given recent advances in genomic technology and organized efforts from peer experts, standardized cytogenomic diagnosis and evidence-based clinical management could be envisioned for all patients with RCs.Furthermore, supernumerary small ring chromosomes and the patients perspective are addressedthe latter by including family stories of RC-carrier relatives. Acquired RCs in various cancers are also discussed, as well as the potential role of RCs in research applications like iPSC cellular modeling and genomic editing.This book is a valuable reference for clinical geneticists, personnel in cytogenetics and molecular genetics laboratories, genetic counselors, and researchers in related fields. Shipping may be from multiple locations in the US or from the UK, depending on stock availability.
