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HIV testing and antiretroviral treatment strategies for prevention of HIV infection: impact on antiretroviral drug resistance

Journal of internal medicine, 2011-12, Vol.270 (6), p.532-549

2011

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Identification of a Gene That Causes Primary Open Angle Glaucoma

Science (American Association for the Advancement of Science), 1997-01, Vol.275 (5300), p.668-670

1997

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Outcomes for people with TB by disease severity at presentation

The international journal of tuberculosis and lung disease, 2024-03, Vol.28 (3), p.142-147

2024

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Managing multidrug-resistant tuberculosis in South Africa: a budget impact analysis

The international journal of tuberculosis and lung disease, 2020-04, Vol.24 (4), p.376-382

2020

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Allelic Variation in the VMD2 Gene in Best Disease and Age-Related Macular Degeneration

Investigative ophthalmology & visual science, 2000-05, Vol.41 (6), p.1291-1296

2000

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Non-targeted HIV screening in emergency departments in the Netherlands

Netherlands journal of medicine, 2017-11, Vol.75 (9), p.386-393

2017

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A 2 base pair deletion in the RDS gene associated with butterfly-shaped pigment dystrophy of the fovea

Human molecular genetics, 1993-05, Vol.2 (5), p.601-603

1993

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Genetic linkage of autosomal dominant neovascular inflammatory vitreoretinopathy to chromosome 11q13

Human molecular genetics, 1992-12, Vol.1 (9), p.685-689

1992

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Fine mapping of the autosomal dominant juvenile open angle glaucoma (GLC1A) region and evaluation of candidate genes

Genome research, 1996-09, Vol.6 (9), p.862-869

1996

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

Nature genetics, 1993-05, Vol.4 (1), p.47-50

1993

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Three autosomal dominant corneal dystrophies map to chromosome 5q

Nature genetics, 1994-01, Vol.6 (1), p.47-51

1994

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Evaluation of a Significantly Shorter Version of the Farnsworth-Munsell 100-Hue Test in Patients with Three Different Optic Neuropathies

Journal of neuro-ophthalmology, 1997-03, Vol.17 (1), p.1-6

1997

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

Nature genetics, 1993-03, Vol.3 (3), p.202-207

1993

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Genetic linkage of vitelliform macular degeneration (Best's disease) to chromosome 11q13

Nature genetics, 1992-07, Vol.1 (4), p.246-250

1992

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Regional distribution of retinal degeneration in patients with the proline to histidine mutation in codon 23 of the rhodopsin gene

Ophthalmology (Rochester, Minn.), 1991-12, Vol.98 (12), p.1806-1813

1991

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A user-friendly Hypercard interface for human linkage analysis

Bioinformatics, 1993-12, Vol.9 (6), p.757-759

1993

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Refining the locus for Best vitelliform macular dystrophy and mutation analysis of the candidate gene ROM1

American journal of human genetics, 1994, Vol.54 (1), p.95-103

1994

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Prostaglandin binding activity and myoblast fusion in aggregates of avian myoblasts

Developmental biology, 1986, Vol.113 (1), p.40-48

1986

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HIV testing and antiretroviral treatment strategies for prevention of HIV infection: impact on antiretroviral drug resistance: Symposium: Prevention of HIV based on test and treat

Journal of internal medicine, 2011-12, Vol.270 (6), p.532-549

2011

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Clinical features of a Stargardt-like dominant progressive macular dystrophy with genetic linkage to chromosome 6q

Archives of ophthalmology (1960), 1994-06, Vol.112 (6), p.765

1994

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A 2 base pair deletion in the RDS gene associated with butterfly-shaped pigment dystrophy of the fovea

Human molecular genetics, 1993-08, Vol.2 (8), p.1347-1347

1993

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Some Corrections of L'Année Littéraire

The Modern language journal (Boulder, Colo.), 1930-10, Vol.15 (1), p.56-56

Nichols, E. B.

1930

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A 2 base bair deletion in the RDS gene associated with butterfly-shaped pigment dystrophy of the fovea

Human molecular genetics, 1993-08, Vol.2 (8), p.1347-1347

1993

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Procollagen II gene mutation in Stickler syndrome

Archives of ophthalmology (1960), 1992-11, Vol.110 (11), p.1589

1992

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West Ford radar and microwave equipment

Proceedings of the IEEE, 1964-01, Vol.52 (5), p.576-588

1964

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HIV testing and antiretroviral treatment strategies for prevention of HIV infection: impact on antiretroviral drug resistance

Identification of a Gene That Causes Primary Open Angle Glaucoma

Outcomes for people with TB by disease severity at presentation

Managing multidrug-resistant tuberculosis in South Africa: a budget impact analysis

Allelic Variation in the VMD2 Gene in Best Disease and Age-Related Macular Degeneration

Non-targeted HIV screening in emergency departments in the Netherlands

A 2 base pair deletion in the RDS gene associated with butterfly-shaped pigment dystrophy of the fovea

Genetic linkage of autosomal dominant neovascular inflammatory vitreoretinopathy to chromosome 11q13

Fine mapping of the autosomal dominant juvenile open angle glaucoma (GLC1A) region and evaluation of candidate genes

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

Three autosomal dominant corneal dystrophies map to chromosome 5q

Evaluation of a Significantly Shorter Version of the Farnsworth-Munsell 100-Hue Test in Patients with Three Different Optic Neuropathies

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

Genetic linkage of vitelliform macular degeneration (Best's disease) to chromosome 11q13

Regional distribution of retinal degeneration in patients with the proline to histidine mutation in codon 23 of the rhodopsin gene

A user-friendly Hypercard interface for human linkage analysis

Refining the locus for Best vitelliform macular dystrophy and mutation analysis of the candidate gene ROM1

Prostaglandin binding activity and myoblast fusion in aggregates of avian myoblasts

HIV testing and antiretroviral treatment strategies for prevention of HIV infection: impact on antiretroviral drug resistance: Symposium: Prevention of HIV based on test and treat

Clinical features of a Stargardt-like dominant progressive macular dystrophy with genetic linkage to chromosome 6q

A 2 base pair deletion in the RDS gene associated with butterfly-shaped pigment dystrophy of the fovea

Some Corrections of L'Année Littéraire

A 2 base bair deletion in the RDS gene associated with butterfly-shaped pigment dystrophy of the fovea

Procollagen II gene mutation in Stickler syndrome

West Ford radar and microwave equipment

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