Genomic disorders : the genomic basis of disease / edited by James R. Lupski, Pawe1 Stankiewicz.
نوع المادة :![نص](/opac-tmpl/lib/famfamfam/BK.png)
- 1588295591 (alk. paper)
- 9781588295590
- 616.042 G E D 22
نوع المادة | المكتبة الحالية | رقم الاستدعاء | رقم النسخة | حالة | تاريخ الاستحقاق | الباركود |
---|---|---|---|---|---|---|
كتاب | المكتبة المركزية | 616.042 G E D (استعراض الرف(يفتح أدناه)) | 1 | Not For Loan | 070083071 | |
كتاب | المكتبة المركزية | 616.042 G E D (استعراض الرف(يفتح أدناه)) | 2 | المتاح | 070083072 | |
كتاب | المكتبة المركزية | 616.042 G E D (استعراض الرف(يفتح أدناه)) | 3 | المتاح | 070083073 | |
كتاب | المكتبة المركزية | 616.042 G E D (استعراض الرف(يفتح أدناه)) | 4 | المتاح | 070083074 | |
كتاب | المكتبة المركزية | 616.042 G E D (استعراض الرف(يفتح أدناه)) | 5 | المتاح | D_11A69 |
Includes bibliographical references and index.
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 al.] -- Ancient transposable elements, processed pseudogenes, and endogenous retroviruses / Adam Pavlicek and Jerzy Jurka -- Segmental duplications / Andrew J. Sharp and Evan E. Eichler -- Non-B DNA and chromosomal rearrangements / Albino Bacolla and Robert D. Wells -- Genetic basis of olfactory deficits / Idan Menashe, Ester Feldmesser, and Doron Lancet -- Genomic organization and function of human centromeres / Huntington F. Willard and M. Katharine Rudd -- Primate chromosome evolution / Stefan Mوuller -- Genome plasticity in evolution: the centromere repositioning / Mariano Rocchi and Nicoletta Archidiacono --
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 / Pawe1 Stankiewicz, Weimin Bi, and James R. Lupski -- Chromosome 22q11.2 rearrangement disorders / Bernice E. Morrow -- Neurofibromatosis 1 / Karen Stephens -- Williams-Beuren syndrome / Stephen W. Scherer and Lucy R. Osborne -- Sotos syndrome / Naohiro Kurotaki and Naomichi Matsumoto -- X chromosome rearrangements / Pauline H. Yen -- Pelizaeus-Merzbacher disease and spastic paraplegia type 2 / Ken Inoue -- Y-chromosomal rearrangements and azoospermia / Matthew E. Hurles and Chris Tyler-Smith --
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 -- Mechanisms underlying neoplasia-associated genomic rearrangements / Thoas Fioretos -- Recombination hotspots in nonallelic homologous recombination / Matthew E. Hurles and James R. Lupski -- Position effects / Pawe1 Stankiewicz -- Chromosome-engineered mouse models / Pentao Liu -- Array-CGH for the analysis of constitutional genomic rearrangements / Nigel P. Carter ... [et al.] -- Appendix A: Well-characterized rearrangement-based diseases and genome structural features at the locus / Pawe1 Stankiewicz and James R. Lupski -- Appendix B: Diagnostic potential for chromosome microarray analysis / Pawe1 Stankiewicz, Sau W. Cheung and Arthur L. Beaudet.
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