Literature DB >> 18134442

Congenital blindness (pseudoglioma) occurring as a sex-linked developmental anomaly.

W M G WILSON.   

Abstract

Entities:  

Keywords:  BLINDNESS; HEREDITY/human

Mesh:

Year:  1949        PMID: 18134442      PMCID: PMC1591533     

Source DB:  PubMed          Journal:  Can Med Assoc J        ISSN: 0008-4409            Impact factor:   8.262


× No keyword cloud information.
  10 in total

1.  Physical anthropology and medicine.

Authors:  J L ANGEL
Journal:  J Natl Med Assoc       Date:  1963-03       Impact factor: 1.798

2.  Inherited retinal detachment.

Authors:  J LEVY
Journal:  Br J Ophthalmol       Date:  1952-11       Impact factor: 4.638

3.  Linkage analysis of Norrie disease with X-chromosomal ornithine aminotransferase.

Authors:  J B Bateman
Journal:  Trans Am Ophthalmol Soc       Date:  1992

4.  Unusual retinal detachment possibly sex-linked.

Authors:  A SORSBY; M KLEIN; J H GANN; G SIGGINS
Journal:  Br J Ophthalmol       Date:  1951-01       Impact factor: 4.638

5.  Discordant monozygotic twins with retinoblastoma and cleft palate.

Authors:  N F WALKER
Journal:  Am J Hum Genet       Date:  1950-12       Impact factor: 11.025

6.  Norrie's disease in an Asian family.

Authors:  D G Harendra de Silva; D B de Silva
Journal:  Br J Ophthalmol       Date:  1988-01       Impact factor: 4.638

7.  Norrie's disease in North America.

Authors:  F C Blodi; W S Hunter
Journal:  Doc Ophthalmol       Date:  1969       Impact factor: 2.379

8.  Dominantly inherited unilateral retinal dysplasia.

Authors:  I C Lloyd; A Colley; A B Tullo; R Bonshek
Journal:  Br J Ophthalmol       Date:  1993-06       Impact factor: 4.638

9.  Dominant exudative vitreoretinopathy and other vascular developmental disorders of the peripheral retina.

Authors:  C E van Nouhuys
Journal:  Doc Ophthalmol       Date:  1982-09-23       Impact factor: 2.379

10.  Probably Norrie's disease due to mutation. Two sporadic sibships of two males each, a necropsy of one case, and, given Norrie's disease, a calculation of the gene mutation frequency.

Authors:  C I Phillips; M Newton; J Duvall; S Holloway; A M Levy
Journal:  Br J Ophthalmol       Date:  1986-04       Impact factor: 4.638

  10 in total

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