%0 Generic
%T Genomic Disorders The Genomic Basis of Disease
%A Lupski, James R.
%A Stankiewicz, Pawel
%I Humana Press Inc
%@ 9781597450393
%K Medicine
%K Pathology
%K Medicine & Public Health
%K Genetic Diseases, Inborn
%K Chromosome Aberrations
%K Genome Components
%K Genome
%K Genomics methods
%K Erbkrankheit
%K Chromosomenaberration
%K Genom
%D 2006
%X Includes bibliographical references and index
%X Front Matter; The CMT1A Duplication; Alu Elements; The Impact of LINE-1 Retro transposition on the Human Genome; Ancient Transposable Elements, Processed Pseudogenes, and Endogenous Retroviruses; Segmental Duplications; Non-B DNA and Chromosomal Rearrangements; Genetic Basis of Olfactory Deficits; Genomic Organization and Function of Human Centromeres; Primate Chromosome Evolution; Genome Plasticity in Evolution; The CMT1A Duplication and HNPP Deletion; Smith-Magenis Syndrome Deletion, Reciprocal Duplication dup(17)(p11.2p11.2), and Other Proximal 17p Rearrangements
%X Chromosome 22q11.2 Rearrangement DisordersNeurofibromatosis 1; Williams-Beuren Syndrome; Sotos Syndrome; X Chromosome Rearrangements; Pelizaeus-Merzbacher Disease and Spastic Paraplegia Type 2; Y-Chromosomal Rearrangements and Azoospermia; Inversion Chromosomes; Monosomy 1p36 As a Model for the Molecular Basis of Terminal Deletions; inv dup(15) and inv dup(22); Mechanisms Underlying Neoplasia-Associated Genomic Rearrangements; Recombination Hotspots in Nonallelic Homologous Recombination; Position Effects; Chromosome-Engineered Mouse Models
%X Array-CGH for the Analysis of Constitutional Genomic RearrangementsBack Matter
%C Humana Press Inc
%C Totowa, NJ
%U http://slubdd.de/katalog?TN_libero_mab2
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