Basic Genetics: A Human Approach

abnormal adenine affected allele amino acids amniocentesis autosomal Barr body bases birth blood BRCA1 BRCA2 breast cancer carrier cause cDNA cells CF gene chance child chro chromo codons condition counselor cytosine detect develop doctor dominant Emmet environment enzyme female fetus Ff Ff Ff Figure frequency gene pool genetic counseling genetic disorders geneticist genome genotype groups growth hormone HD gene hemoglobin hGH gene human genetics inactivation individuals infants inherited karyotype Lisa male meiosis Mendel ment mitosis molecule mosome mother mRNA mutation netic nontasters normal nucleotides occur offspring ovarian cancer pairs parents pedigree percent person plasmid pop beads population pregnancy prenatal diagnosis probability problems produce protein quencies recessive gene recessive trait result retarded risk scientists screening sequence sex chromosomes sickle sickle-cell disease sperm strand symptoms syndrome thymine tion twins variation Worksheet X chromosome X-linked