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Inguinal hernia and atrial septal defect in tel Hashomer camptodactyly syndrome: Report of a new case expanding the phenotypic spectrum of the disease |
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| Authors: | P. Franceschini M. P. Vardeu F. Signorile A. Testa A. Guala D. Franceschini L. Dalforno |
| Affiliation: | Istituto di Discipline Pediatriche, Servizio di Genetica Clinica, Università di Torino, Torino, Italy |
| Abstract: | |
| Keywords: | autosomal recessive inheritance connective tissue defect pleiotropic effects |