Literature DB >> 4954614

[The different types of sclerocornea, their hereditary modes and concomitant congenital malformations].

N Bloch.   

Abstract

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Mesh：

Year:  1965        PMID： 4954614

Source DB:  PubMed          Journal:  J Genet Hum        ISSN： 0021-7743


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  5 in total

1.  Clinicopathological correlation of congenital corneal opacification using ultrasound biomicroscopy.

Authors:  K K Nischal; J Naor; V Jay; L D MacKeen; D S Rootman
Journal:  Br J Ophthalmol       Date:  2002-01       Impact factor: 4.638

2.  The genetics of cornea plana congenita.

Authors:  E Tahvanainen; H Forsius; J Kolehmainen; M Damsten; J Fellman; A de la Chapelle
Journal:  J Med Genet       Date:  1996-02       Impact factor: 6.318

3.  Sclerocornea associated with the chromosome 22q11.2 deletion syndrome.

Authors:  Gil Binenbaum; Donna M McDonald-McGinn; Elaine H Zackai; B Michael Walker; Karlene Coleman; Amy M Mach; Margaret Adam; Melanie Manning; Deborah M Alcorn; Carrie Zabel; Dennis R Anderson; Brian J Forbes
Journal:  Am J Med Genet A       Date:  2008-04-01       Impact factor: 2.802

4.  An epidemiological investigation of a Forkhead box protein E3 founder mutation underlying the high frequency of sclerocornea, aphakia, and microphthalmia in a Mexican village.

Authors:  Carlos Pantoja-Melendez; Manir Ali; Juan C Zenteno
Journal:  Mol Vis       Date:  2013-08-27       Impact factor: 2.367

5.  A Cohesin Subunit Variant Identified from a Peripheral Sclerocornea Pedigree.

Authors:  Bi Ning Zhang; Tommy Chung Yan Chan; Pancy Oi Sin Tam; Yu Liu; Chi Pui Pang; Vishal Jhanji; Li Jia Chen; Wai Kit Chu
Journal:  Dis Markers       Date:  2019-11-12       Impact factor: 3.434
  5 in total

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