This full-color, coil-bound flipbook contains graphics with captions covering the most common topics in human genetics including: amniocentesis, anaphase lag, anatomical line drawings (digestive tract, urinary tract, brain, spinal cord, etc), autosomal dominant/recessive inheritance, balanced reciprocal translocations, cancer, chromosome nomenclature, karyotypes, chorionic villus sampling (CVS), confined placental mosaicism (CPM), duplication/deletion syndromes, heart defects (ASD, VSD, coarctation of the aorta), hemizygosity, imprinting, iversions, linkage analysis, meiosis, mitosis, metabolic disorders, mitochondrial disorders, monosomy, mosaicism, multifactorial disorders, nondisjunction, percutaneous umbilical blood sampling (PUBS), uniparental disomy (UPD), prenatal maternal serum screening (Triple & Quad test), Rh sensitization, Rd disease, Robertsonian translocations, trinucleotide repeat disorders, trisomy, twinning, X inactivation (lyonization), X-linked recessive inheritance, and X-linked recessive traits. Available in English, Spanish and French Editions.