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Mutation in the RIEG1 Gene in Patients with Iridogoniodysgenesis Syndrome

Human molecular genetics, 1998-07, Vol.7 (7), p.1113-1117

1998

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Mutation of the PAX6 gene in patients with autosomal dominant keratitis

American journal of human genetics, 1995-09, Vol.57 (3), p.539-548

1995

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On the Malleability of Performance: Implications for Seniors

Journal of applied gerontology, 2008-08, Vol.27 (4), p.446-465

2008

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A summary of 20 CACNA1F mutations identified in 36 families with incomplete X-linked congenital stationary night blindness, and characterization of splice variants

Human genetics, 2001-02, Vol.108 (2), p.91-97

2001

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Autosomal dominant iridogoniodysgenesis anomaly maps to 6p25

American journal of human genetics, 1996-12, Vol.59 (6), p.1321-1327

1996

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Autosomal-dominant Iridogoniodysgenesis and Axenfeld-Rieger Syndrome are Genetically Distinct

Ophthalmology (Rochester, Minn.), 1996-11, Vol.103 (11), p.1907-1915

1996

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Evidence for Genetic Heterogeneity in X-Linked Congenital Stationary Night Blindness

American journal of human genetics, 1998-04, Vol.62 (4), p.865-875

1998

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Tracking ability in subjects symptomatic of cumulative trauma disorder: does it relate to disability?

Ergonomics, 2001-03, Vol.44 (4), p.443-456

2001

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Identification of the Human Chromosomal Region Containing the Iridogoniodysgenesis Anomaly Locus by Genomic-Mismatch Scanning

American journal of human genetics, 1997-07, Vol.61 (1), p.111-119

1997

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Localization of a gene for incomplete X-linked congenital stationary night blindness to the interval between DXS6849 and DXS8023 in Xp11.23

Human genetics, 1998-08, Vol.103 (2), p.124-130

1998

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Manifestations of X-linked congenital stationary night blindness in three daughters of an affected male : demonstration of homozygosity

American journal of human genetics, 1993, Vol.52 (1), p.71-77

1993

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Variability of iris defects in autosomal dominant aniridia

Canadian journal of ophthalmology, 1994-02, Vol.29 (1), p.25-29

PEARCE, W. G

1994

Volltextzugriff (PDF)

Unexpected stereoacuity following surgical correction of long-standing horizontal strabismus

Canadian journal of ophthalmology, 1993-08, Vol.28 (5), p.217-220

1993

Volltextzugriff (PDF)

Variable expressivity in X-linked congenital stationary night blindness

Canadian journal of ophthalmology, 1990-02, Vol.25 (1), p.3-10

1990

Volltextzugriff (PDF)

Inferior rectus muscle restriction after retrobulbar anesthesia for cataract extraction

Canadian journal of ophthalmology, 1989-06, Vol.24 (4), p.162-165

1989

Volltextzugriff (PDF)

Autosomal dominant keratitis: a possible aniridia variant

Canadian journal of ophthalmology, 1995-04, Vol.30 (3), p.131-137

1995

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Autosomal dominant megalocornea with congenital glaucoma : evidence for germ-line mosaicism

Canadian journal of ophthalmology, 1991-02, Vol.26 (1), p.21-26

PEARCE, W. G

1991

Volltextzugriff (PDF)

Clinical variability among patients with incomplete X-linked congenital stationary night blindness and a founder mutation in CACNA1F

Canadian journal of ophthalmology, 2000-06, Vol.35 (4), p.204-213

2000

Volltextzugriff (PDF)

Loss-of-function mutations in a calcium-channel α1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness

Nature genetics, 1998-07, Vol.19 (3), p.264-267

1998

Volltextzugriff (PDF)

A locus for X-linked congenital stationary night blindness is located on the proximal portion of the short arm of the X chromosome

Human genetics, 1990-04, Vol.84 (5), p.406-408

1990

Volltextzugriff (PDF)

Incidence of accommodative impairment following traumatic hyphema

Canadian journal of ophthalmology, 1993-10, Vol.28 (6), p.263-265

1993

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Recession of the superior oblique tendon in A-pattern strabismus

Canadian journal of ophthalmology, 1990-10, Vol.25 (6), p.301-305

1990

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Mapping of locus for X-linked congenital stationary night blindness (CSNB1) proximal to DXS7

Genomics (San Diego, Calif.), 1992-02, Vol.12 (2), p.409-411

1992

Volltextzugriff (PDF)

Corneal involvement in autosomal dominant coloboma/microphthalmos

Canadian journal of ophthalmology, 1986-12, Vol.21 (7), p.291-294

PEARCE, W. G

1986

Volltextzugriff (PDF)

Gene locus for X-linked CSNB

Genomics (San Diego, Calif.), 1990-12, Vol.8 (4), p.743-743

1990

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Mutation in the RIEG1 Gene in Patients with Iridogoniodysgenesis Syndrome

Mutation of the PAX6 gene in patients with autosomal dominant keratitis

On the Malleability of Performance: Implications for Seniors

A summary of 20 CACNA1F mutations identified in 36 families with incomplete X-linked congenital stationary night blindness, and characterization of splice variants

Autosomal dominant iridogoniodysgenesis anomaly maps to 6p25

Autosomal-dominant Iridogoniodysgenesis and Axenfeld-Rieger Syndrome are Genetically Distinct

Evidence for Genetic Heterogeneity in X-Linked Congenital Stationary Night Blindness

Tracking ability in subjects symptomatic of cumulative trauma disorder: does it relate to disability?

Identification of the Human Chromosomal Region Containing the Iridogoniodysgenesis Anomaly Locus by Genomic-Mismatch Scanning

Localization of a gene for incomplete X-linked congenital stationary night blindness to the interval between DXS6849 and DXS8023 in Xp11.23

Manifestations of X-linked congenital stationary night blindness in three daughters of an affected male : demonstration of homozygosity

Variability of iris defects in autosomal dominant aniridia

Unexpected stereoacuity following surgical correction of long-standing horizontal strabismus

Variable expressivity in X-linked congenital stationary night blindness

Inferior rectus muscle restriction after retrobulbar anesthesia for cataract extraction

Autosomal dominant keratitis: a possible aniridia variant

Autosomal dominant megalocornea with congenital glaucoma : evidence for germ-line mosaicism

Clinical variability among patients with incomplete X-linked congenital stationary night blindness and a founder mutation in CACNA1F

Loss-of-function mutations in a calcium-channel α1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness

A locus for X-linked congenital stationary night blindness is located on the proximal portion of the short arm of the X chromosome

Incidence of accommodative impairment following traumatic hyphema

Recession of the superior oblique tendon in A-pattern strabismus

Mapping of locus for X-linked congenital stationary night blindness (CSNB1) proximal to DXS7

Corneal involvement in autosomal dominant coloboma/microphthalmos

Gene locus for X-linked CSNB

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