REVIEWS Williams Syndrome As a Model for

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Syndromes Rare diseases Molecular biology Williams syndrome LIMK1 Cofilin 1 Mutation Gene duplication Epigenetics Biology Genetics Proteins		REVIEWS Williams Syndrome As a Model for Add to Reading List Source URL: www.ncbi.nlm.nih.gov Download Document from Source Website File Size: 551,00 KB Share Document on Facebook

	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
	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