Clinical features of five pedigrees genetically linked to the juvenile glaucoma locus on chromosome 1q21-q31 (Q73212560)

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2 November 2019

title

Clinical features of five pedigrees genetically linked to the juvenile glaucoma locus on chromosome 1q21-q31 (English)

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2 November 2019

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J L Wiggs

1

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2 November 2019

E A Del Bono

2

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2 November 2019

J S Schuman

3

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2 November 2019

B T Hutchinson

4

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2 November 2019

D S Walton

5

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2 November 2019

publication date

1 December 1995

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2 November 2019

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2 November 2019

volume

102

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2 November 2019

issue

12

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2 November 2019

page(s)

1782-1789

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Dominant goniodysgenesis with late congenital glaucoma. A re-examination of Berg's pedigree

2 November 2019

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Privacy rules blindside French glaucoma effort

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Clinical features and linkage analysis of a family with autosomal dominant juvenile glaucoma

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Familial glaucoma. In nine generations of a South Hampshire family

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Iridoschisis as a cause of glaucoma

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7 January 2021

Genetic linkage of familial open angle glaucoma to chromosome 1q21–q31

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7 January 2021

Familial hypoplasia of the iris stroma associated with glaucoma

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7 January 2021

Genetic linkage of autosomal dominant juvenile glaucoma to 1q21-q31 in three affected pedigrees

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7 January 2021

Ocular findings in patients with autosomal dominant retinitis pigmentosa and a rhodopsin gene defect (Pro-23-His).

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7 January 2021

Butterfly-shaped pigment dystrophy of the fovea caused by a point mutation in codon 167 of the RDS gene

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7 January 2021

Mutations at the PAX6 locus are found in heterogeneous anterior segment malformations including Peters' anomaly

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Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants

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A second-generation linkage map of the human genome

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The 1993-94 Généthon human genetic linkage map

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Identifiers

DOI

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2 November 2019

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