Literature DB >> 5678778

[Hereditary arthro-ophthalmopathy].

J Spranger.   

Abstract

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Mesh：

Year:  1968        PMID： 5678778

Source DB:  PubMed          Journal:  Ann Radiol (Paris)        ISSN： 0003-4185


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  6 in total

1.  A constitutional disorder of connective tissue suggesting a defect in collagen biosynthesis.

Authors:  W N Meigel; P K Müller; B F Pontz; N Sörensen; J Spranger
Journal:  Klin Wochenschr       Date:  1974-10-01

Review 2.  The Wagner-Stickler syndrome complex.

Authors:  V Godel; P Nemet; M Lazar
Journal:  Doc Ophthalmol       Date:  1981-12-16       Impact factor: 2.379

3.  Syndromes of genetic juvenile retinal detachment.

Authors:  R J Gorlin; W H Knobloch
Journal:  Z Kinderheilkd       Date:  1972

4.  Stickler syndrome. Report of a second Australian family.

Authors:  K Kozlowski; G Turner
Journal:  Pediatr Radiol       Date:  1975-09-15

5.  The Stickler syndrome presenting as a dominantly inherited cleft palate and blindness.

Authors:  J G Hall; H Herrod
Journal:  J Med Genet       Date:  1975-12       Impact factor: 6.318

6.  Inherited hyaloideoretinopathy and skeletal dysplasia.

Authors:  W H Knobloch
Journal:  Trans Am Ophthalmol Soc       Date:  1975
  6 in total

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