An Introduction to Human Genetics |
Contents
Chapter One INTRODUCTION AND HISTORICAL | 1 |
CONTENTS | 2 |
Chapter Two MENDELIAN INHERITANCE | 9 |
Copyright | |
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abnormal Acad activity affected persons albino alleles amino acid antibodies antigens autosomal blood centromere chemical chromatid chromo cleft co-workers codon complement complex culture defect deletion diploid disease dominant Down's syndrome Drosophila enzyme example F₁ factors families females fetal fibroblasts Figure frequency function G6PD gametes genotype gonadal haploid hemoglobin heredity heterozygotes heterozygous homologous homozygous human chromosomes Human Genet inheritance involving karyotype known linkage loci locus males malformations markers mating meiosis meiotic Mendelian metabolic molecule mRNA mutation mutation rate nondisjunction normal nucleotides observed occur offspring pairs parents patients pedigree percent phenotype polypeptide chain population produced protein ratio recessive recombination red cells regions replication residue result ribosomes segregation sequence sex chromosomes sibships single somatic specific ẞ chain structural gene studies synthesis tion tissues traits translocation trisomy Turner's syndrome twins variation X chromosome X-linked zygote