Advances in Genetics, Volume 33
Academic Press, Nov 14, 1995 - Science - 336 pages
Advances in Genetics increases its focus on modern human genetics and its relation to medicine with Volume 33 of this long-standing serial. The recent merger of Molecular Genetic Medicine with Advances in Genetics affirms the Academic Press commitment to publish important reviews of the broadest interest to geneticists and their colleagues in affiliated disciplines.
In this volume, Petes and Pukkila synthesize the latest research on meiotic recombination, with specific reference to crossover and gene conversions. The "absurd size and complex" structure of the Dystrophin gene is considered in another chapter, with discussions of strategies for future diagnosis and treatment of muscular dystrophy. Two chapters also examine the molecular genetics of sex determination, including the influence of maternal age and resulting chromosomal aberrations. Volume 33 also includes a review of the PAX and HOX gene families and their links to the developmental process, cellular growth control, and forms of cancer. Case studies of thrombophilia, Menkes, and Wilson diseases are used to exemplify the genetic disorders of blood clotting, copper deficiency, and toxicity, respectively. Triman takes a genetic approach to understanding the function of ribosomal RNA using E. coli as the model best able to reveal the inherent complications of the translation process. Leach and O'Connell describe the use of radiation hybrids for constructing high-resolution maps of the human genome. With these reviews the alliance of Molecular Genetic Medicine with Advances in Genetics is completed under the banner of Advances in Genetics.
* Presents technical and historical overviews of molecular biology applied to disease detection, diagnosis, and treatment
* Chronicles the continuing explosion of knowledge in molecular genetic medicine by highlighting current approaches to understanding human illness
* Documents the revolution in human and molecular genetics leading to a new field of medicine
* This volume highlights Analysis of human chromosomes with chapters on pathology of sex determination and numerical chromosomal abnormalities Molecular and genetic bases of muscular dystrophy and Menkes and Wilson diseases Techniques including FISH, IRS-PCR, and radiation hybrids
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Chapter 2 Meiotic Sister Chromatid Recombination
Chapter 4 The Origin of Numerical Chromosome Abnormalities
The Discovery of Activated Protein C Resistance
Chapter 6 Dystrophin Its Gene and the Dystrophinopathies
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16S ribosomal RNA 16S rRNA abnormalities Acad analysis anticoagulant APC resistance assay associated autosomal binding Biol cDNA Cell Cambridge chromo chromosome 21 clones containing copper crossovers cytogenetic Dahlback Dahlberg deﬁciency deletion detected disease gene domain Duchenne muscular dystrophy dystrophin dystrophin gene encodes Escherichia coli exons expression factor V gene ﬁrst function Genet genomic gonadal dysgenesis Goodfellow human chromosome identiﬁed interaction involved isolated linkage loci locus markers maternal age meiosis meiotic membrane Menkes disease mice molecular mouse muscle mutagenesis Natl Nature London nondisjunction nonsister normal observed pair patients PAX genes phenotype plasma plasmid polymorphisms Proc radiation hybrid radiation hybrid map radiation hybrid panel recombination region ribosomal RNA sequences sex chromosome sex determination sex reversal signiﬁcant sister chromatid skeletal SOX9 speciﬁc structure studies subunit syndrome testis thrombosis tion tissue transcription translocation trisomy tumor Wilson disease XX males XY females Y chromosome