Genomic disorders :  the genomic basis of disease / 
edited by James R. Lupski, Pawe� Stankiewicz. 
 - Totowa, N.J. :  Humana Press,  c2006. 
 - xvii, 426 p. :  ill. (some col.) ;  27 cm. 
<br/><br/>Includes bibliographical references and index. 
<br/><br/>Inversion chromosomes / Orsetta Zuffardi ... [et al.] -- Monosomy 1p36 as a model for the molecular basis of terminal deletions / Blake C. Ballif and Lisa G. Shaffer -- Inv dup(15) and inv dup(22) / Heather E. McDermid and Rachel Wevrick -- Mech The CMT1A duplication and HNPP deletion / Vincent Timmerman and James R. Lupski -- Smith-Magenis syndrome deletion, reciprocal duplication dup(17)(p11.2p11.2), and other proximal 17p rearrangements / Pawe� Stankiewicz, Weimin Bi, and Jame The CMT1A duplication: a historical perspective viewed from two sides of an ocean / James R. Lupski and Vincent Timmerman -- Alu elements / Prescott Deininger -- The impact of LINE-1 retrotransposition on the human genome / Amy E. Hulme ... [et  
<br/><br/><label>ISBN: </label>1588295591 (alk. paper) 9781588295590 
<br/><br/><label>LCCN: </label>2005020461 
<br/><br/><label>Nat. Bib. Agency Control No.: </label>101252812  DNLM 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Genetic disorders--Molecular aspects.<br/>Genetic Diseases, Inborn.<br/>Chromosome Aberrations.<br/>Genome Components.<br/>Genome.<br/>Genomics--methods.
<br/><br/><label>LC Class. No.: </label>RB155.5  / .G46-2006 
<br/><br/><label>Dewey Class. No.: </label>616/.042 
<br/><br/><label>National Library of Medicine Call No.: </label>QZ 50  / G3354 2006