Human Molecular GeneticsHuman Molecular Genetics 2 Tom Strachan & Andrew P. Read "truly a Rolls Royce amongst textbooks" — Molecular Medicine Today "the best text to introduce students and scientists to the molecular aspects of human genetics" — Trends in Genetics "a beautifully crafted book" — Journal of Medical Genetics "addresses the gap between introductory textbooks and the primary literature. There’s no other textbook quite like it." — Nature Now extensively rewritten and updated, HMG2 guides students and researchers through the very latest developments in the most rapidly changing area of life science. The highly regarded structure of the bestselling first edition is retained, but a wealth of new data and features have been added to aid understanding of the principles of human molecular genetics:
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Problems and Solutions for Strachan and Read's Human Molecular Genetics 2 David James Matthes,Andrew Read No preview available - 2001 |
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abnormal active affected alleles amino acid amplification analysis autosomal bands binding cancer cDNA centromere chain chromatids coding DNA codon complex containing copies CpG islands crossover database deletion DNA cloning DNA fragments DNA sequences DNA strand dominant duplication dystrophin elements encode enzyme eukaryotic example exons Figure frequency function gene expression gene families genomic DNA homologs human chromosomes human genome hybridization identified imprinting inactivation individual inherited insert introns involves labeled linkage located loci locus mammalian mapping markers mechanism meiosis membrane mendelian methylation mitochondrial molecular molecules mouse mRNA mtDNA mutations normal nucleic acid nucleotide occur oligonucleotide pattern phenotype polymorphisms polypeptide population primer probe promoter protein pseudogenes receptor region replication restriction result RNA polymerase rRNA screening Section segments signal single somatic specific splicing structure syndrome synthesis tandem repeats target DNA tion tissue transcription factors translocation tRNA tumor vector X chromosome