(Q34185704)

31 July 2017

title

Clinicopathologic correlation and genetic analysis in a case of posterior polymorphous corneal dystrophy (English)

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posterior polymorphous corneal dystrophy

31 July 2017

main subject

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13

Michael Boehnke

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31 July 2017

Sayoko E Moroi

1

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31 July 2017

Parag A Gokhale

2

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31 July 2017

Miriam T Schteingart

3

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31 July 2017

Alan Sugar

4

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31 July 2017

Catherine A Downs

5

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31 July 2017

Satoko Shimizu

6

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31 July 2017

Charles Krafchak

7

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31 July 2017

Nobuo Fuse

8

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31 July 2017

Susan G Elner

9

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31 July 2017

Victor M Elner

10

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31 July 2017

Andrew Flint

11

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31 July 2017

Michael P Epstein

12

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31 July 2017

Julia E Richards

14

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31 July 2017

language of work or name

English

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publication date

1 April 2003

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American Journal of Ophthalmology

31 July 2017

published in

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31 July 2017

volume

135

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31 July 2017

issue

4

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31 July 2017

page(s)

461-470

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The Clinical Spectrum of Posterior Polymorphous Dystrophy

31 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2802%2902032-9

Glaucoma due to endothelialization of the anterior chamber angle. A comparison of posterior polymorphous dystrophy of the cornea and Chandler's syndrome

7 January 2021

1 reference

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Open-angle glaucoma associated with posterior polymorphous dystrophy. A clinicopathologic study.

7 January 2021

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Linkage of posterior polymorphous corneal dystrophy to 20q11

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2802%2902032-9

VSX1: a gene for posterior polymorphous dystrophy and keratoconus

7 January 2021

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Missense mutations in COL8A2, the gene encoding the alpha2 chain of type VIII collagen, cause two forms of corneal endothelial dystrophy

7 January 2021

1 reference

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Clinical phenotype of juvenile-onset primary open-angle glaucoma linked to chromosome 1q.

7 January 2021

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Linkage of congenital hereditary endothelial dystrophy to chromosome 20.

7 January 2021

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Initial sequencing and analysis of the human genome

7 January 2021

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Localization of the gene for autosomal recessive congenital hereditary endothelial dystrophy (CHED2) to chromosome 20 by homozygosity mapping

7 January 2021

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Programs for pedigree analysis: Mendel, Fisher, and dGene

7 January 2021

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Detection and integration of genotyping errors in statistical genetics

7 January 2021

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PedCheck: a program for identification of genotype incompatibilities in linkage analysis

7 January 2021

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Structure, development and function of cytoskeletal elements in non-neuronal cells of the human eye.

7 January 2021

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Immunohistochemical analysis of the pathogenesis of posterior polymorphous dystrophy

7 January 2021

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Characterization of a hormone-producing ovarian carcinoma cell line

7 January 2021

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Alport syndrome. A review of the ocular manifestations

7 January 2021

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Exclusion of AR-CHED from the chromosome 20 region containing the PPMD and AD-CHED loci

7 January 2021

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Posterior polymorphous membranous dystrophy with overlapping features of iridocorneal endothelial syndrome

7 January 2021

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The barrier function in neodymium-YAG laser capsulotomy.

7 January 2021

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Epithelial downgrowth following phacoemulsification through a clear cornea

7 January 2021

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A comparison of the clinical variations of the iridocorneal endothelial syndrome

7 January 2021

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Electron microscopy of posterior polymorphous degeneration

7 January 2021

1 reference

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Morphologic characteristics of posterior polymorphous dystrophy. A study of nine corneas and review of the literature

7 January 2021

1 reference

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Early-onset posterior polymorphous dystrophy

7 January 2021

1 reference

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Genetics of the corneal dystrophies: what we have learned in the past twenty-five years

7 January 2021

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Advances in the molecular genetics of corneal dystrophies

7 January 2021

1 reference

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Comprehensive human genetic maps: individual and sex-specific variation in recombination

7 January 2021

1 reference

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10.1016/S0002-9394(02)02032-9

7 January 2021

Identifiers

DOI

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31 July 2017

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