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Genomic disorders : the genomic basis of disease / edited by James R. Lupski, Pawe� Stankiewicz.

Contributor(s): Material type: TextTextPublication details: Totowa, N.J. : Humana Press, c2006.Description: xvii, 426 p. : ill. (some col.) ; 27 cmISBN:
  • 1588295591 (alk. paper)
  • 9781588295590
Subject(s): DDC classification:
  • 616/.042 22
LOC classification:
  • RB155.5 .G46-2006
NLM classification:
  • QZ 50
Online resources:
Contents:
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
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Holdings
Item type Current library Call number Status Date due Barcode
Book Book Dr. Panjwani Center for Molecular Medicine and Drug Research (PCMD) Library RB-155.5-.G46-2006 (Browse shelf(Opens below)) Available P 718
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RM-301.25-.A63-2006 Analogue-based drug discovery / R-733-.C65-2006 Complementary medicine in clinical practice : QP-551-.P76-2006 Protein design : RB-155.5-.G46-2006 Genomic disorders : QH-430-.L48-2008 Genes IX / RC115-.S77-2003 Clinical Bacteriology QH-430-.L48-2008 Genes IX /

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