Normal view MARC view ISBD view

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.

Includes bibliographical references and index.

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

ISBN: 1588295591 (alk. paper) 9781588295590

LCCN: 2005020461

Nat. Bib. Agency Control No.: 101252812 DNLM

Subjects--Topical Terms:
Genetic disorders--Molecular aspects.
Genetic Diseases, Inborn.
Chromosome Aberrations.
Genome Components.
Genome.
Genomics--methods.

LC Class. No.: RB155.5 / .G46-2006

Dewey Class. No.: 616/.042

National Library of Medicine Call No.: QZ 50 / G3354 2006