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Medical Genetics and the Physician
Chromosomal Basis of Inheritance
Chemical Basis of Inheritance
16 other sections not shown
agents Amer amino acid analysis anemia anomalies aortic associated autosomal dominant autosomal recessive Bartalos biochemical defects blood cancer carcinogenic cardiovascular carrier causes cell division cent chemical child chromo chromosomal aberrations Chromosome studies congenital heart disease congenital malformations culture Cytogenetics Decr deficiency diagnosis disorders drug dwarfism environment enzyme female fetal frequently galactosemia genetic counseling genetic defects genetic diseases genetic factors genetic information genetic material gonadal growth hemoglobin hereditary histidinemia hormone human inborn errors inherited involved karyotype Lancet m-RNA male Marfan syndrome McKusick medical genetics Medicine meiosis meiotic mental retardation metabolic diseases mongolism mutations normal nucleotide occur offspring organs parents patients pattern Pediatrics pedigree phenotype phenylketonuria physician polypeptide polypeptide chain present produce reaction recurrence risk result serum sex chromatin sex chromosome sickle cell somatic cells spontaneous abortions stenosis structural syndrome tion tissue trait translocation trisomy Turner's syndrome urinary urine usually variations