Literature DB >> 4213898

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

W G Bradley, J Richardson, I J Frew.   

Abstract

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Year:  1974        PMID： 4213898     DOI： 10.1093/brain/97.1.521

Source DB:  PubMed          Journal:  Brain        ISSN： 0006-8950            Impact factor:   13.501


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  4 in total

1.  A case of neurofibromatosis 2 presenting with a mononeuritis multiplex.

Authors:  T J Kilpatrick; R J Hjorth; M F Gonzales
Journal:  J Neurol Neurosurg Psychiatry       Date:  1992-05       Impact factor: 10.154

2.  Genetic mapping of X-linked albinism-deafness syndrome (ADFN) to Xq26.3-q27.I.

Authors:  Y Shiloh; G Litvak; Y Ziv; T Lehner; L Sandkuyl; M Hildesheimer; V Buchris; F P Cremers; P Szabo; B N White
Journal:  Am J Hum Genet       Date:  1990-07       Impact factor: 11.025

3.  An unusual combination of unilateral orbital plexiform neurofibroma in a patient with oculocutaneous albinism.

Authors:  J Saravanan; A Rajendraprasad; S Priyadharshni
Journal:  Indian J Ophthalmol       Date:  2014-06       Impact factor: 1.848

4.  Coincidence of neurofibromatosis and myotonic dystrophy in a kindred.

Authors:  K Ichikawa; C J Crosley; A Culebras; L Weitkamp
Journal:  J Med Genet       Date:  1981-04       Impact factor: 6.318
  4 in total

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