THE FAMILIAL ASSOCIATION OF NEUROFIBROMATOSIS, PERONEAL MUSCULAR ATROPHY, CONGENITAL DEAFNESS, PARTIAL ALBINISM, AND AXENFELD'S DEFECT

Abstract
W. G. BRADLEY, J. RICHARDSON, I. J. C. FREW; THE FAMILIAL ASSOCIATION OF NEUROFIBROMATOSIS, PERONEAL MUSCULAR ATROPHY, CONGENITAL DEAFNESS, PARTIAL ALBINISM, A

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