Product Code Database
   » » Barcode: 9780124046313
Tag Barcode '9780124046313'.
Tag
Mark as Favorite

Benign & Pathological Chromosomal Imbalances: Microscopic And Submicroscopic Copy Number Variations (cnvs) In Genetics And Counseling
 (

No Synopsis Available


Specifications
  • Benign and Pathological Chromosomal Imbalances: Microscopic and Submicroscopic Copy Number Variations (Cnvs) in Genetics and Counseling available on October 27 2022 from BiggerBooks for 92.66
  • Benign & Pathological Chromosomal Imbalances: Microscopic And Submicroscopic Copy Number Variations (cnvs) In Genetics And Counseling available on August 17 2018 from VitalSource for Https://www.vitalsource.com/en-au/textbooks?term=9780124046313&cjsku=9780124046313" itemprop="offers" target="_external" title="" itemscope itemtype="http://schema.org/Offer">107.23
  • ISBN bar code 9780124046313 ξ1 registered October 27 2022
  • ISBN bar code 9780124046313 ξ2 registered April 02 2017
  • Product category is Book

  • # 9780124046313R
  • # 9780124046313

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 achieve the promise of universal coverage or cost efficacy to sample investigated, deep chromosome analysis and molecular cytogenetics remains relevant for technology translation, study design, and therapeutic assessment. Knowledge of the rare but recurrent rearrangements unfamiliar to practitioners saves time and money for molecular cytogeneticists and genetics counselors, helping to distinguish benign from harmful CG-CNV. It also supports them in deciding which molecular cytogenetics tools to deploy. Shows how to define the inheritance and formation of cytogenetically visible copy number variations using cytogenetic and molecular approaches for genetic diagnostics, patient counseling, and treatment plan developmentUniquely classifies all known variants by chromosomal origin, saving time and money for researchers in reviewing benign and pathologic variants before costly molecular methods are used to investigateSide-by-side comparison of copy number variants with their recently identified submicroscopic form, aiding technology assessment using aCGH and other techniques


References
    ^ (2015). Benign and Pathological Chromosomal Imbalances: Microscopic and Submicroscopic Copy Number Variations (Cnvs) in Genetics and Counseling BiggerBooks. (revised Oct 2022)
    ^ Benign & Pathological Chromosomal Imbalances: Microscopic And Submicroscopic Copy Number Variations (cnvs) In Genetics And Counseling VitalSource. (revised Aug 2018)

Page 1 of 1
1

Account

Social:
Pages:  ..   .. 
Items:  .. 

Navigation

General: Atom Feed Atom Feed  .. 
Help:  ..   .. 
Category:  ..   .. 
Media:  ..   .. 
Posts:  ..   ..   .. 

Statistics

Page:  .. 
Summary:  .. 
1 Tags
7/10 Page Rank
400 Page Refs
5s Time
32 Sources