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ON THE USE OF THE CATALOGS
Nosologic and Other Tables
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abnormal absence affected persons affected sibs alleles alpha anomaly antigen Arch aspartic acid associated ataxia atrophy autosomal dominant autosomal dominant inheritance autosomal recessive beta bilateral Biochem Birth Defects blood group bone brachydactyly Brit brothers cataract Child chromosome cleft Clin Clinical Delineation congenital consanguinity corneal cystinosis deafness deficiency dehydrogenase Delineation of Birth Dermatol described a family disease disorder dwarfism dysplasia dystrophy Ehlers-Danlos syndrome enzyme family study father females gene Genet glutamic acid HEMOGLOBIN hemolytic anemia Hereditary heterozygotes human hypoplasia kindred Lancet Lehmann lesions linkage loci locus lysine male-to-male transmission males malformations McKusick mental retardation metabolism mother multiple mutation Neurol Neurology normal º º º observed occurs onset Ophthal Ophthalmol parents patients Pediat pedigree personal communication phenotype polydactyly polymorphism proband Proc protein recessive inheritance red cell renal reported serum showed sibships sister skin suggested Surg syndactyly syndrome variant X-linked