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Problems in Human Genetics by Barton Childs
DNA by F H C Crick
Mutations and the Control of Protein Structure
10 other sections not shown
abnormal Acad alleles amino acid Biochem Biol blood cent chain Chem chemical child chromatin-positive chromo chronic irradiation Clin colour-blind condition congenital Crick de-phospho-enzyme defect deficiency deleterious diabetes disease dose drastic Drosophila melanogaster effect enzyme enzyme activity erythrocytes evidence females fertility fetal hemoglobin Figure flies frequency G-6-P dehydrogenase galactose galactose-l-phosphate galactosemia gene genetic genotype glucose glucose-6-phosphate dehydrogenase gonadal dysgenesis gonadal dysplasia hemo hemolysates heterosis heterozygotes heterozygous homozygous human hypothesis idiogram inbreeding individuals induced Ingram inhibition Klinefelter's syndrome Lancet lethal loci locus males mating mechanism Medical metabolic mice molecular molecule mongolism mutation rate Neel non-disjunction normal observed obtained occur pair patients with Klinefelter's peptide phenotype phosphate phosphoglucomutase Polani population possible primaquine primaquine-sensitive problem Proc protein radiation reaction recessive red cells Russell sensitive sex chromosome shown spermatogonia studies tion tissue trisomy Turner's syndrome viability wildtype x-ray