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  • Title: Guadalajara camptodactyly syndrome. A distinct probably autosomal recessive disorder.
    Author: Cantú JM, Rivera H, Nazará Z, Rojas Q, Hernández A, García-Cruz D.
    Journal: Clin Genet; 1980 Sep; 18(3):153-9. PubMed ID: 7192193.
    Abstract:
    Two sisters, aged 18 and 11 years, were found to have an intrauterine growth retardation-malformation syndrome which included camptodactyly as a typical sign. The overall analysis of the clinical and radiological findings permitted the individualization of a distinct entity. The family data suggested autosomal recessive inheritance.
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