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Heritability of Diseases and Traits
Chromosomal Basis of Heredity
Autosomal Chromosomal Anomalies
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abnormal affected allele amino acid anemia aneuploidy antibody antigen appears autosomal dominant autosomal recessive band Barr bodies beta biochemical birth blood group cancer cardiovascular cause cells centromere chain Chapter child chromatin chromo chromosomal anomaly cleft lip clinical congenital heart crease deafness deficiency dermatoglyphic disorder drome drugs environmental enzyme example factors fected female fetal frequency genetic counseling genotype heart disease hemoglobin heritability heterozygote heterozygous homozygote homozygous human inborn errors increased individual infant inheritance involved karyotype lesions loci locus long arm male malformations mendelian mental retardation metabolism molecule mother multifactorial mutant mutant gene netic Noonan syndrome normal occur pairs palate parents patients pattern phenotype polypeptide population pregnancy proband produced protein recurrence risk relatives rubella septal defect serum sibs skin somatic specific stenosis studies Table teratogenic thalassemia tients tion tissue trait translocation trisomy Turner syndrome twins X chromosome X-linked