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CHAPTER PAGE 1 The Study of Human Heredity
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abnormal affected Agglutinated albinism alleles allergy anemia antibody antigen appears ataxia autosomal blood groups cancer carrier cause cells cent chapter child chorea clinical color-blind condition congenital court crossing-over daughters DDee deafness dementia praecox dependent diagnosis disorders dominant factor dominant gene dwarfism enuresis environment environmental evidence family history father females FRIEDREICH'S ATAXIA Gaucher's disease genetic basis genetic factor genotype gland goitre hemophilia hemophilic hereditary behavior hereditary factors heredity heterozygous human heredity Huntington's chorea hypothyroid identical twins incompletely sex-linked individuals involves kinds of hereditary known linkage Macklin males medical genetics mental traits mother muscular atrophy MYOTONIA CONGENITA normal occurs onset optic atrophy pair of chromosomes parents patient pedigree person physician pigmented psoriasis psychosis rare recessive factor recessive gene recorded reduced penetrance result Retinitis sclerosis serum sex-linked SEX-LINKED GENES sex-linked recessive show the trait skin specific susceptibility tests thyroid tion trauma tumors usually variations various Y-chromosome