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10.1002/ajmg.1320100308.abs We report a new autosomal dominant condition involving hands and feet of an Arabic father and 5 of his 11 children. This trait is characterized by symphalangism, syndactyly, brachydactyly type D, clinodactyly, and hypoplasia of the thenar and hypothenar eminences....
10.1002/ajmg.1320100312.abs Two adult Black sibs with homozygous β‐thalassemia had severe deficiency of β‐chain production but an unusually mild clinical course and almost normal hematocrit values. Their father had the typical hematological findings of β‐thalassemia trait but the mother,...
10.1002/ajmg.1320100310.abs A “bingo” model is one in which the pattern of survival of a system is determined by whichever of several components, each with its own particular distribution for survival, fails first. The model is motivated by the study of lifespan in animals. A number of...
10.1002/ajmg.1320100307.abs The records of an ongoing Health Surveillance Registry that utilizes multiple sources of ascertainment were used to study the incidence rate of infantile hypertrophic pyloric stenosis (IHPS) in liveborn children in British Columbia during the period 1966–1977...
10.1002/ajmg.1320100305.abs Eight children from seven presumably unrelated families were identified independently as having an unbalanced recombinant chromosome resulting in the presence of extra material on the short arm of a chromosome 8. Parental chromosomes were analyzed, and one member of...
10.1002/ajmg.1320100304.abs Genetic aspects of IgE levels were studied in three large pedigrees, many of whose members had atopic sensitivities to ragweed. Data on 184 persons (80 M, 104 F) were analyzed by the methods of Elston and Stewart after logarithmic transformation and appropriate...
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