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MEDICAL GENETICS 1958
New Books Journals Symposia and Congresses
79 other sections not shown
A.M.A. Arch abnormal Acta genet affected allele amino acid anemia anomalies antigen association autosomal dominant autosomal recessive basis blood group bone Brit cancer cent child chromosome Clin clinical Coauthors colleagues described congenital consanguinity cystic defect deficiency demonstrated diagnosis discussed disorder dominant trait dysplasia enzyme erythrocyte evidence excretion factor female fetal fetal hemoglobin frequency galactosemia gene globulin gonadal haptoglobins hemoglobin hemolytic hemophilia hereditary Heredity heterozygotes heterozygous homozygous Human Genet hypertension hypophosphatasia inheritance Klinefelter syndrome Lancet linkage male malformations Marfan syndrome medical genetics metabolism Mongolism mother multiple mutation Negro normal observed occurred offspring parents patients Pediatrics pedigree persons phenotype phenylketonuria plasma population porphyria pregnancy present probands protein recessive trait red cells relatives renal reported result reviewed rheumatoid serum sex chromatin sex-linked siblings sibships sickle cell studied suggested thalassemia tissue tumor Turner syndrome urinary urine Wilson's disease X chromosome