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GENES AND CONGENITAL
CHROMOSOMES AND CONGENITAL
6 other sections not shown
46 chromosomes abnormal allele Acad agammaglobulinemia allele amino acid antibody antigen autosomal blood group cancer carcinoma cause cent chains chemical chromo clinical condition congenital Courtesy Dr defect deficiency disorder enzyme erythrocytes factor female fraction function galactose galactosemia gene frequency genotype germ cell globulins glucose glycogen gonadal hemoglobin hemolytic hemophilia heredity heterozygote heterozygous heterozygous carriers homozygotes Human Genet hypothesis immune incidence infants infection karyotype Klinefelter's syndrome Lancet leukemia linkage loci locus male mating meiosis meiotic Mendelian metabolic mice mitotic molecule mosaicism mutants mutation rate nondisjunction normal nucleic acid occur parents patients peptides permission of author phenotype phenylalanine population present Proc produce protein recessively inherited recombination ribosomes selection serum sickle-cell anemia skin somatic specific structural genes studies suggesting syndrome synthesis Tay-Sachs disease thalassemia tion tissue translocation trisomy tumor Turner's syndrome twins viral virus viruses vitro X chromosome X-linked y-globulin