The familial association of neurofibromatosis, peroneal muscular atrophy, congenital deafness, partial albinism, and axenfeld's defect

Walter G Bradley, J. Richardson, I. J C Frew

Research output: Contribution to journalArticle

14 Citations (Scopus)
Original languageEnglish (US)
Pages (from-to)21-532
Number of pages512
JournalBrain
Volume97
Issue number3
DOIs
StatePublished - 1974
Externally publishedYes

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Piebaldism
Charcot-Marie-Tooth Disease
Neurofibromatoses
Deafness
Defects
Familial

ASJC Scopus subject areas

  • Clinical Neurology

Cite this

The familial association of neurofibromatosis, peroneal muscular atrophy, congenital deafness, partial albinism, and axenfeld's defect. / Bradley, Walter G; Richardson, J.; Frew, I. J C.

In: Brain, Vol. 97, No. 3, 1974, p. 21-532.

Research output: Contribution to journalArticle

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