TY - GEN
AU - Lupski, James R.
AU - Stankiewicz, Pawel
TI - Genomic Disorders The Genomic Basis of Disease
PB - Humana Press Inc
SN - 9781597450393
KW - Medicine
KW - Pathology
KW - Medicine & Public Health
KW - Genetic Diseases, Inborn
KW - Chromosome Aberrations
KW - Genome Components
KW - Genome
KW - Genomics methods
KW - Erbkrankheit
KW - Chromosomenaberration
KW - Genom
PY - 2006
N2 - Includes bibliographical references and index
N2 - 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
N2 - 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
N2 - Array-CGH for the Analysis of Constitutional Genomic RearrangementsBack Matter
BT - SpringerLink ; Bücher
CY - Totowa, NJ
ER -
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