Wyniki wyszukiwania:
wyszukanych pozycji: 22
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Fluorescence in Situ Hybridization (Fish): Application Guide
ISBN: 9783662571002 / Angielski / Miękka / 2018 / 606 str. Termin realizacji zamówienia: ok. 16-18 dni roboczych. |
cena:
563,56 |
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Human Genetics : A Basic Training Package
ISBN: 9783746797465 / Angielski / Miękka / 2018 / 168 str. Termin realizacji zamówienia: ok. 10-14 dni roboczych. Overall, this book is meant as a kind of 'starter package' for interested future human genetics specialists.
Overall, this book is meant as a kind of 'starter package' for interested future human genetics specialists.
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cena:
49,20 |
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Cytogenomics
ISBN: 9780128235799 / Angielski / Miękka / 2021 Termin realizacji zamówienia: ok. 16-18 dni roboczych. |
cena:
666,89 |
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Small supernumerary marker chromosomes
ISBN: 9783758451935 / Angielski / Miękka / 108 str. Termin realizacji zamówienia: ok. 10-14 dni roboczych. This book is essential information for those affected, their families, and doctors who are confronted with the diagnosis, that they are dealing with a small supernumerary marker chromosome (= sSMC). This book clarifies basic questions on the subject such as: - What are sSMCs and how are they structured? - What genetic parts do they consist of? - What is known about the nature of sSMC formation? - How is an sSMC diagnosed? - What clinical problems do they cause? - How are they categorized? - What are the effects of cell mosaics? - What are familial or de novo sSMCs? - Why does uniparental...
This book is essential information for those affected, their families, and doctors who are confronted with the diagnosis, that they are dealing with a...
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cena:
89,42 |
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Fluorescence in Situ Hybridization (Fish) - Application Guide
ISBN: 9783642089527 / Angielski / Miękka / 2010 / 451 str. Termin realizacji zamówienia: ok. 16-18 dni roboczych. This application guide provides an overview of the principles and basic techniques of fluorescence in situ hybridization (FISH) and primed in situ hybridization (PRINS), which are successfully used to study many aspects of genomic behavior and alterations.
This application guide provides an overview of the principles and basic techniques of fluorescence in situ hybridization (FISH) and primed in situ hyb...
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cena:
724,58 |
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All you need to know about uniparental disomy
ISBN: 9783758465581 / Angielski / Miękka / 116 str. Termin realizacji zamówienia: ok. 10-14 dni roboczych. 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...
This book is aimed at anyone interested in the biological phenomenon of uniparental disomy (UPD). Since UPD can lead to congenital diseases, this is ...
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cena:
134,15 |
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Uniparental Disomy (Upd) in Clinical Genetics: A Guide for Clinicians and Patients
ISBN: 9783662511145 / Angielski / Miękka / 2016 / 192 str. Termin realizacji zamówienia: ok. 16-18 dni roboczych. This book focus on genetic diagnostics for Uniparental Disomy (UPD), a chromosomal disorder defined by the exceptional presence of a chromosome pair derived from only one parent, which leads to a group of rare diseases in humans.
This book focus on genetic diagnostics for Uniparental Disomy (UPD), a chromosomal disorder defined by the exceptional presence of a chromosome pair d...
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cena:
402,53 |
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Kleine überzählige Marker-Chromosomen
ISBN: 9783758451669 / Niemiecki / Miękka / 108 str. Termin realizacji zamówienia: ok. 10-14 dni roboczych. Dieses Buch ist eine grundlegende Information für Betroffene, deren Familien, und Ärzte, die mit der Diagnose konfrontiert sind, dass sie es mit einem kleinen überzähligen Marker-Chromosom (engl. small supernumerary marker chromosome = sSMC) zu tun haben. In diesem Buch werden grundlegenden Fragen zum Thema geklärt wie: - Was sind sSMCs und wie sind sie aufgebaut? - Aus welchen genetischen Anteilen bestehen sie? - Was ist über die Art der sSMC-Bildung bekannt? - Wie wird ein sSMC diagnostiziert? - Welche klinischen Probleme verursachen sie? - Wie teilt man sie ein? - Welche Auswirkungen...
Dieses Buch ist eine grundlegende Information für Betroffene, deren Familien, und Ärzte, die mit der Diagnose konfrontiert sind, dass sie es mit ein...
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cena:
89,42 |
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Alles, was man über Uniparentale Disomie wissen muss
ISBN: 9783758465574 / Niemiecki / Miękka / 116 str. Termin realizacji zamówienia: ok. 10-14 dni roboczych. Das vorliegende Buch richtet sich an alle am biologischen Phänomen der uniparentale Disomie (UPD) Interessierte. Dass die UPD auch zu angeborenen Erkrankungen führen kann, ist ebenfalls ein wichtiges Thema des Buches - es sind acht Erfahrungsberichte betroffener Familien im Buch wieder gegeben.Es werden mit dem Buch folgende und weitere Fragen beantwortet: - Was ist eine UPD?- Was unterscheidet angeborene und erworbene UPD?- Wie häufig ist das UPD-Phänomen?- Wie kann eine UPD entstehen?- Welche Formen der UPD gibt es?- Wie wirkt UPD sich klinisch aus?- Ist UPD erblich?- Wie kann man UPD...
Das vorliegende Buch richtet sich an alle am biologischen Phänomen der uniparentale Disomie (UPD) Interessierte. Dass die UPD auch zu angeborenen Erk...
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cena:
134,15 |
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Benign and Pathological Chromosomal Imbalances: Microscopic and Submicroscopic Copy Number Variations (Cnvs) in Genetics and Counseling
ISBN: 9780124046313 / Angielski / Twarda / 2013 / 199 str. Termin realizacji zamówienia: ok. 16-18 dni roboczych. Benign & Pathological Chromosomal Imbalances systematically clarifies the disease implications of cytogenetically visible copy number variants (CG-CNV) using cytogenetic assessment of heterochromatic or euchromatic DNA variants. While variants of several megabasepair can be present in the human genome without clinical consequence, visually distinguishing these benign areas from disease implications does not always occur to practitioners accustomed to costly molecular profiling methods such as FISH, aCGH, and NGS. As technology-driven approaches like FISH and aCGH have yet to... Benign & Pathological Chromosomal Imbalances systematically clarifies the disease implications of cytogenetically visible copy number varian... |
cena:
335,83 |
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Fluorescence in Situ Hybridization (Fish): Application Guide
ISBN: 9781071651490 / Angielski Termin realizacji zamówienia: ok. 10-14 dni roboczych. |
cena:
1018,44 |
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Fluorescence in Situ Hybridization (Fish): Application Guide
ISBN: 9783662529577 / Angielski / Twarda / 2016 / 606 str. Termin realizacji zamówienia: ok. 10-14 dni roboczych. This manual offers detailed protocols for fluorescence in situ hybridization (FISH) and comparative genomic hybridization approaches, which have been successfully used to study various aspects of genomic behavior and alterations. Methods using different probe and cell types, tissues and organisms, such as mammalians, fish, amphibians (including lampbrush-chromosomes), insects, plants and microorganisms are described in 57 chapters. In addition to multicolor FISH procedures and special applications such as the characterization of marker chromosomes, breakpoints, cryptic aberrations, nuclear... This manual offers detailed protocols for fluorescence in situ hybridization (FISH) and comparative genomic hybridization approaches, which have be... |
cena:
814,74 |
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Pukas : Über die nächsten Verwandten des 'großen weißen Hasen' bekannt aus "Mein Freund Harvey" / About the next relatives of the 'big white rabbit' known from "Harvey"
ISBN: 9783746723853 / Niemiecki / Miękka / 2018 / 60 str. Termin realizacji zamówienia: ok. 10-14 dni roboczych. Nahezu jeder kennt den großen weißen Hasen Harvey aus dem Film "Mein Freund Harvey" mit James Stewart.
Nahezu jeder kennt den großen weißen Hasen Harvey aus dem Film "Mein Freund Harvey" mit James Stewart.
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cena:
55,20 |
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Pequenos cromossomos marcadores supranumerários
ISBN: 9783758454387 / Portugalski / Miękka / 108 str. Termin realizacji zamówienia: ok. 10-14 dni roboczych. |
cena:
89,42 |
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Small Supernumerary Marker Chromosomes (sSMC): A Guide for Human Geneticists and Clinicians
ISBN: 9783642207655 / Angielski / Twarda / 2011 / 242 str. Termin realizacji zamówienia: ok. 16-18 dni roboczych. Human beings normally have a total of 46 chromosomes, with each chromosome present twice, apart from the X and Y chromosomes in males. Some three million people worldwide, however, have 47 chromosomes: they have a small supernumerary marker chromosome (sSMC) in addition to the 46 normal ones. This sSMC can originate from any one of the 24 human chromosomes and can have different shapes. Approximately one third of sSMC carriers show clinical symptoms, while the remaining two thirds manifest no phenotypic effects. This guide represents the first book ever published on this topic. It presents...
Human beings normally have a total of 46 chromosomes, with each chromosome present twice, apart from the X and Y chromosomes in males. Some three mill...
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cena:
442,79 |
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Petits marqueurs chromosomiques surnuméraires
ISBN: 9783758458576 / Francuski / Miękka / 108 str. Termin realizacji zamówienia: ok. 10-14 dni roboczych. Ce livre est une information fondamentale pour les personnes concernées, leurs familles, et les médecins confrontés au diagnostic, qu'ils l'ont fait avec un petit marqueur chromosomique surnuméraire (Angl. small supernumerary marker chromosome = sSMC). Ce livre répond à des questions fondamentales sur le sujet, telles que :- Que sont les sSMC et comment sont-ils structurés ? - De quelles parties génétiques se composent-ils ? - Que sait-on sur le mode de formation des sSMC ? - Comment un sSMC est-il diagnostiqué ? - Quels problèmes cliniques provoquent-ils ? - Comment les...
Ce livre est une information fondamentale pour les personnes concernées, leurs familles, et les médecins confrontés au diagnostic, qu'ils l'ont fai...
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cena:
89,42 |
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Uniparental Disomy (Upd) in Clinical Genetics: A Guide for Clinicians and Patients
ISBN: 9783642552878 / Angielski / Twarda / 2014 / 192 str. Termin realizacji zamówienia: ok. 16-18 dni roboczych. This book focus on genetic diagnostics for Uniparental Disomy (UPD), a chromosomal disorder defined by the exceptional presence of a chromosome pair derived from only one parent, which leads to a group of rare diseases in humans. First the molecular and cytogenetic background of UPD is described in detail; subsequently, all available information of the various chromosomal origins and the latest findings on genotype-phenotype correlations and clinical consequences are discussed. Numerous personal reports from families with a child suffering from a UPD-induced syndrome serve to... This book focus on genetic diagnostics for Uniparental Disomy (UPD), a chromosomal disorder defined by the exceptional presence of a chromosome pai... |
cena:
563,56 |
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Pookas : About the next relatives of the 'big white rabbit' known from "Harvey"
ISBN: 9783746743936 / Niemiecki / Miękka / 2018 / 36 str. Termin realizacji zamówienia: ok. 10-14 dni roboczych. Almost everyone knows the big white rabbit Harvey from the movie "Harvey" with James Stewart...
Almost everyone knows the big white rabbit Harvey from the movie "Harvey" with James Stewart...
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cena:
55,20 |
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Humangenetik : Eine grundlegende Trainingseinheit - Edition 2020
ISBN: 9783750276154 / Niemiecki Termin realizacji zamówienia: ok. 10-14 dni roboczych. Dieses Buch stellt einen allgemeinen Überblick über die Humangenetik dar.
Dieses Buch stellt einen allgemeinen Überblick über die Humangenetik dar.
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cena:
53,68 |
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Human Genetics : A Basic Training Package Edition 2020
ISBN: 9783750276123 / Angielski Termin realizacji zamówienia: ok. 10-14 dni roboczych. This book is a general overview on Human Genetics.
This book is a general overview on Human Genetics.
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cena:
53,68 |
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