Literature DB >> 5489095

Hereditary nystagmus in early childhood.

B Harcourt.   

Abstract

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Year:  1970        PMID： 5489095      PMCID： PMC1468883          DOI： 10.1136/jmg.7.3.253

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  1 in total

1.  Role of electroretinography in investigation of impaired visual function in childhood.

Authors:  K Wybar; B Harcourt
Journal:  Arch Dis Child       Date:  1968-12       Impact factor: 3.791
  1 in total
  5 in total

1.  A gene for X-linked idiopathic congenital nystagmus (NYS1) maps to chromosome Xp11.4-p11.3.

Authors:  A Cabot; J M Rozet; S Gerber; I Perrault; D Ducroq; A Smahi; E Souied; A Munnich; J Kaplan
Journal:  Am J Hum Genet       Date:  1999-04       Impact factor: 11.025

2.  Congenital nystagmus: a clinical perspective in infancy.

Authors:  S S Gelbart; C S Hoyt
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1988       Impact factor: 3.117

Review 3.  Nystagmus in infancy.

Authors:  I Casteels; C M Harris; F Shawkat; D Taylor
Journal:  Br J Ophthalmol       Date:  1992-07       Impact factor: 4.638

4.  Value of the ERG in congenital nystagmus.

Authors:  P A Good; A E Searle; S Campbell; S J Crews
Journal:  Br J Ophthalmol       Date:  1989-07       Impact factor: 4.638

5.  Fast-phase instabilities in normally sighted relatives of congenital nystagmus patients--autosomal dominant and x-chromosome recessive modes of inheritance.

Authors:  J Shallo-Hoffmann; D Watermeier; J Petersen; H Mühlendyck
Journal:  Neurosurg Rev       Date:  1988       Impact factor: 3.042
  5 in total

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