Literature DB >> 5020170

Clefting syndromes associated with retinal detachment.

W H Knobloch, J M Layer.   

Abstract

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Year:  1972        PMID： 5020170     DOI： 10.1016/0002-9394(72)90003-7

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


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  10 in total

1.  Genetic linkage analysis of hereditary arthro-ophthalmopathy (Stickler syndrome) and the type II procollagen gene.

Authors:  R G Knowlton; E J Weaver; A F Struyk; W H Knobloch; R A King; K Norris; A Shamban; J Uitto; S A Jimenez; D J Prockop
Journal:  Am J Hum Genet       Date:  1989-11       Impact factor: 11.025

2.  Wagner's syndrome.

Authors:  A Pinckers; L M Jansen
Journal:  Doc Ophthalmol       Date:  1974-11       Impact factor: 2.379

Review 3.  The Wagner-Stickler syndrome complex.

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

Review 4.  Brain malformations associated with Knobloch syndrome--review of literature, expanding clinical spectrum, and identification of novel mutations.

Authors:  Ahmet Okay Caglayan; Jacob F Baranoski; Fesih Aktar; Wengi Han; Beyhan Tuysuz; Aslan Guzel; Bulent Guclu; Hande Kaymakcalan; Berrin Aktekin; Gozde Tugce Akgumus; Phillip B Murray; Emine Z Erson-Omay; Caner Caglar; Mehmet Bakircioglu; Yildirim Bayezit Sakalar; Ebru Guzel; Nihat Demir; Oguz Tuncer; Senem Senturk; Baris Ekici; Frank J Minja; Nenad Šestan; Katsuhito Yasuno; Kaya Bilguvar; Huseyin Caksen; Murat Gunel
Journal:  Pediatr Neurol       Date:  2014-09-04       Impact factor: 3.372

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

7.  Copy number variation analysis implicates the cell polarity gene glypican 5 as a human spina bifida candidate gene.

Authors:  Alexander G Bassuk; Lakshmi B Muthuswamy; Riley Boland; Tiffany L Smith; Alissa M Hulstrand; Hope Northrup; Matthew Hakeman; Jason M Dierdorff; Christina K Yung; Abby Long; Rachel B Brouillette; Kit Sing Au; Christina Gurnett; Douglas W Houston; Robert A Cornell; J Robert Manak
Journal:  Hum Mol Genet       Date:  2012-12-07       Impact factor: 6.150

8.  Hereditary vitreoretinal dystrophy associated with peripheral neuropathy.

Authors:  A Ettl; S Felber; C Kunze; C Schmidauer; B Utermann; A Daxer; W Göttinger
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1994-06       Impact factor: 3.117

9.  Retinal detachment in median cleft-face syndrome.

Authors:  V Feiler-Ofry; V Godel; P Nemet; M Lazar
Journal:  Br J Ophthalmol       Date:  1980-02       Impact factor: 4.638

10.  Autosomal dominant juvenile vitreoretinal degeneration and retinal detachment.

Authors:  K M Saari
Journal:  Int Ophthalmol       Date:  1986-04       Impact factor: 2.031
  10 in total

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