An Introduction to Human Genetics |
Contents
Chapter One INTRODUCTION AND HISTORICAL | 1 |
CONTENTS | 2 |
Chapter Two MENDELIAN INHERITANCE | 9 |
Copyright | |
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Common terms and phrases
abnormal Acad activity albino alleles amino acid anaphase antibodies antigens autosomal banding centromere chro chromatid chromo cleft co-workers codons complement complex crossing culture Cytogenetics cytoplasm defect deletion diploid disease division dominant Down's syndrome Drosophila enzyme example F₁ families females fetal Figure frequency function G6PD gametes genotype gonadal haploid hemoglobin heredity heterozygotes heterozygous homologous homozygous human chromosomes Human Genet inheritance involving isochromosomes karyotype known loci locus long arm males malformations meiosis meiotic Mendel Mendelian metabolic metaphase molecule mosaic mosome mRNA mutation nondisjunction normal nucleotides observed occur offspring pairs parents patients pedigree percent phenotype polypeptide chain population produced protein ratio recessive red cells regions replication result ribosomes segregation sequence sex chromatin sex chromosomes short arm sibships single specific sperm structural gene studies synthesis testicular tion tissues traits translocation trisomy Turner's syndrome twins variation X chromosome X-linked zygote