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Fundamentals of Clinical Genetics
Genetics and Cancer
19 other sections not shown
abnormalities activity adrenal affected alleles amino acid anemia anomalies antigens Arch associated ataxia atrophy autosomal dominant autosomal recessive autosomal recessive trait biochemical Birth Defects bone cancer carcinoma cells childhood chromosome chronic cleft Clin clinical condition congenital corneal cystic cystic fibrosis deafness deficiency deletion described diabetes disease disorder dwarfism dysplasia dystrophy Engl enzymatic enzyme excretion factors female fetal fibroblasts fibrosis frequently gene genetic counseling gonadal hearing loss hemoglobin hepatic hereditary heritable heterogeneity heterozygotes hormone Hum Genet hypoparathyroidism hypoplasia hypoplastic immunodeficiency increased infants involvement karyotype kidney lesions leukemia leukocytes levels liver lymphocytes lysosomal male malformations mental retardation metabolism multiple muscle mutation normal occur onset patients Pediatr pedigree phenotype plasma porphyria prenatal diagnosis protein pulmonary rare recessive inheritance recurrence renal reported result retinal risk serum skin sporadic studies symptoms syndrome Table thyroid tion tissue translocation trisomy tumors Turner syndrome urinary usually variable variant vitamin X-linked recessive