Literature DB >> 5311788

Syndrome of congenital high myopia with nyctalopia. Report of findings in 25 families.

S Merin, H Rowe, E Auerbach, J Landau.   

Abstract

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Year:  1970        PMID： 5311788     DOI： 10.1016/0002-9394(70)90887-1

Source DB:  PubMed          Journal:  Am J Ophthalmol        ISSN： 0002-9394            Impact factor:   5.258


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  7 in total

1.  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

2.  A locus for X-linked congenital stationary night blindness is located on the proximal portion of the short arm of the X chromosome.

Authors:  N T Bech-Hansen; L L Field; A M Schramm; M Reedyk; I W Craig; N J Fraser; W G Pearce
Journal:  Hum Genet       Date:  1990-04       Impact factor: 4.132

3.  Congenital stationary nightblindness.

Authors:  R E Carr
Journal:  Trans Am Ophthalmol Soc       Date:  1974

4.  The autosomal recessive variety of congenital stationary night-blindness with myopia.

Authors:  V M Der Kaloustian; S A Baghdassarian
Journal:  J Med Genet       Date:  1972-03       Impact factor: 6.318

5.  Vision in albinism.

Authors:  C G Summers
Journal:  Trans Am Ophthalmol Soc       Date:  1996

6.  Selective abnormality of the cone B-wave in a patient with retinal degeneration.

Authors:  R Young; J Price; N Gorham; M Cowart
Journal:  Doc Ophthalmol       Date:  1985-08-30       Impact factor: 2.379

7.  A naturally-occurring mutation in Cacna1f in a rat model of congenital stationary night blindness.

Authors:  Yonghao Gu; Lifeng Wang; Jie Zhou; Qun Guo; Na Liu; Zhenqiang Ding; Li Li; Xinping Liu; Jing An; Guolin Yan; Libo Yao; Zuoming Zhang
Journal:  Mol Vis       Date:  2008-01-09       Impact factor: 2.367
  7 in total

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