Genomic Disorders The Genomic Basis of Disease /
It is now abundantly clear that architectural features of the human genome can lead to DNA rearrangements that cause both disease and behavioral traits. In Genomic Disorders: The Genomic Basis of Disease, distinguished experts and pioneers in the field of genomics and genome rearrangements summarize...
| Συγγραφή απο Οργανισμό/Αρχή: | |
|---|---|
| Άλλοι συγγραφείς: | , |
| Μορφή: | Ηλεκτρονική πηγή Ηλ. βιβλίο |
| Γλώσσα: | English |
| Έκδοση: |
Totowa, NJ :
Humana Press,
2006.
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| Θέματα: | |
| Διαθέσιμο Online: | Full Text via HEAL-Link |
Πίνακας περιεχομένων:
- The CMT1A Duplication
- Genomic Structure
- 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
- Genome Evolution
- Primate Chromosome Evolution
- Genome Plasticity in Evolution
- Genomic Rearrangements and Disease Traits
- The CMT1A Duplication and HNPP Deletion
- Smith-Magenis Syndrome Deletion, Reciprocal Duplication dup(17)(p11.2p11.2), and Other Proximal 17p Rearrangements
- Chromosome 22q11.2 Rearrangement Disorders
- Neurofibromatosis 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
- Functional Aspects of Genome Structure
- Recombination Hotspots in Nonallelic Homologous Recombination
- Position Effects
- Genomic Disorders: Modeling And Assays
- Chromosome-Engineered Mouse Models
- Array-CGH for the Analysis of Constitutional Genomic Rearrangements.
