<--- Back to Details
First PageDocument Content
Comparative genomic hybridization / Fluorescence in situ hybridization / Deletion / Human genome / Aneuploidy / Karyotype / Chromosome / Gene duplication / Genetic testing / Biology / Genetics / Cytogenetics
Date: 2007-12-31 10:54:00
Comparative genomic hybridization
Fluorescence in situ hybridization
Deletion
Human genome
Aneuploidy
Karyotype
Chromosome
Gene duplication
Genetic testing
Biology
Genetics
Cytogenetics

Microsoft Word - RCPU news genetic testing.doc

Add to Reading List

Source URL: www.peds.ufl.edu

Download Document from Source Website

File Size: 108,97 KB

Share Document on Facebook

Similar Documents

Reconstruction of Ancestral Gene Order after Segmental Duplication and Gene Loss Jun Huan1 , Jan Prins1 , Wei Wang1 , Todd Vision2 Departments of 1 Computer Science and 2 Biology University of North Carolina at Chapel Hi

DocID: 1viuY - View Document

Gene Duplication to Enable Genetic Programming to Concurrently Evolve Both the Architecture and Work-Performing Steps of a Computer Program John R. Koza Stanford University Computer Science Department Stanford, Californi

DocID: 1u6U1 - View Document

Reconciliation using Duplication, Transfer, and Loss SUPPLEMENTARY MATERIAL For the paper titled “Efficient Algorithms for the Reconciliation Problem with Gene Duplication, Horizontal Transfer, and Loss”, by Mukul S

DocID: 1te89 - View Document

How to find which exon or exons to skip. There is an easy way to find the exon or exons which have to be skipped for your son, if you know the mutation in his dystrophin gene – deletion, duplication, or premature stop.

DocID: 1sVjc - View Document

Muscular dystrophy / Biology / Genetics / Mdx mouse / Clinical medicine / Duchenne muscular dystrophy / Dystrophin / Gene duplication / DMD / Draft:BMN 044 / Draft:SRP-4044

Research Review No. 97. Mice with Exon 2 Duplication. The Studies: The authors of this study note that around 11% of cases of Duchenne Muscular Dystrophy (DMD) are due to a duplication in the dystrophin gene (1). Of th

DocID: 1reMl - View Document