Stickler syndrome: Correlation between vitreoretinal phenotypes and linkage to COL 2A1-Reference-Cited by-同舟云学术

Stickler syndrome: Correlation between vitreoretinal phenotypes and linkage to COL 2A1

Published:1994-11 Issue:6 Volume:8 Page:609-614
ISSN:0950-222X
Container-title:Eye
language:en
Short-container-title:Eye

Author:

Snead Martin P,Payne Stewart J,Barton David E,Yates John R W,Al-Imara Lamya,Popp F Michael,Scott John D

Publisher

Springer Science and Business Media LLC

Subject

Ophthalmology

Link

http://www.nature.com/articles/eye1994153.pdf

Reference24 articles.

1. Stickler GB, Belau PG, Farrell FJ, Jones JD, Pugh DG, Steinberg AG, Ward LE . Hereditary progressive arthro-ophthalmopathy. Mayo Clin Proc 1965;40:433–55.

2. Stickler GB, Pugh DG . Hereditary progressive arthro-oph-thalmopathy. II. Additional observations on vertebral abnormalities, a hearing defect, and a report of a similar case. Mayo Clin Proc 1967;42:495–500.

3. Francomano CA, Liberfarb RM, Hirose T, Maumenee IH, Sreeten EA, Meyers DA, Pyeritz RE . The Stickler syndrome: evidence of close linkage to the structural gene for type II collagen. Genomics 1987;1:293–6.

4. Marshall D . Ectodermal dysplasia. Am J Ophthalmol 1958;45:143–56.

5. Wagner H . Ein bisher unbekanntes Erbleiden des Auges (Degeneratio hyaloideo-retinalis hereditaria), beobachtet im Kanton Zurich. Klin Monatsbl Augenheilkd 1938;100:840–57.

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