UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Molecular genetics and prospects for therapy of the inherited retinal dystrophies

Current Opinion in Genetics & Development, 2001-06, Vol.11 (3), p.307-316

2001

Volltextzugriff (PDF)

Analysis of predictors of success in the MRCP (UK) PACES examination in candidates attending a revision course

Postgraduate medical journal, 2006-02, Vol.82 (964), p.145-149

2006

Volltextzugriff (PDF)

Reduction in intraocular pressure after excimer laser photorefractive keratectomy : Correlation with pretreatment myopia

Ophthalmology (Rochester, Minn.), 1997-03, Vol.104 (3), p.355-359

1997

Volltextzugriff (PDF)

A Mutation in Guanylate Cyclase Activator 1A (GUCA1A) in an Autosomal Dominant Cone Dystrophy Pedigree Mapping to a New Locus on Chromosome 6p21.1

Human molecular genetics, 1998-02, Vol.7 (2), p.273-277

1998

Volltextzugriff (PDF)

Valsalva retinopathy presenting with subhyaloid haemorrhage

Emergency medicine journal : EMJ, 2009-01, Vol.26 (1), p.74-74

2009

Volltextzugriff (PDF)

Phenotype of autosomal recessive congenital microphthalmia mapping to chromosome 14q32

British journal of ophthalmology, 1999-08, Vol.83 (8), p.919-922

1999

Volltextzugriff (PDF)

Genetic analysis of the guanylate cyclase activator 1B (GUCA1B) gene in patients with autosomal dominant retinal dystrophies

Journal of medical genetics, 1999-09, Vol.36 (9), p.691-693

1999

Volltextzugriff (PDF)

A Locus for Autosomal Recessive Congenital Microphthalmia Maps to Chromosome 14q32

American journal of human genetics, 1998-05, Vol.62 (5), p.1113-1116

1998

Volltextzugriff (PDF)

Founder Effect, Seen in the British Population, of the 172 Peripherin/RDS Mutation—and Further Refinement of Genetic Positioning of the Peripherin/RDS Gene

American journal of human genetics, 1998-01, Vol.62 (1), p.192-195

1998

Volltextzugriff (PDF)

Importance of the autosomal recessive retinitis pigmentosa locus on 1q31-q32.1 (RP12) and mutation analysis of the candidate gene RGS16 (RGS-r)

Journal of medical genetics, 2000-05, Vol.37 (5), p.384-387

2000

Volltextzugriff (PDF)

The management of dislocated lens material after phacoemulsification

Eye (London), 1998, Vol.12 (4), p.641-645

1998

Volltextzugriff (PDF)

Lamellar keratoplasty in the management of inflammatory corneal ulceration and perforation

Eye (London), 1994-01, Vol.8 (1), p.22-28

1994

Volltextzugriff (PDF)

Results of Excimer Laser Retreatment of Residual Myopia after Previous Photorefractive Keratectomy

Ophthalmology (Rochester, Minn.), 1997-08, Vol.104 (8), p.1321-1326

1997

Volltextzugriff (PDF)

Astigmatism Induced by Spherical Photorefractive Keratectomy Corrections

Ophthalmology (Rochester, Minn.), 1997-08, Vol.104 (8), p.1317-1320

1997

Volltextzugriff (PDF)

A New Locus for Autosomal Recessive RP (RP29) Mapping to Chromosome 4q32-q34 in a Pakistani Family

Investigative ophthalmology & visual science, 2001-06, Vol.42 (7), p.1436-1438

2001

Volltextzugriff (PDF)

A mutation in NRL is associated with autosomal dominant retinitis pigmentosa

Nature genetics, 1999-04, Vol.21 (4), p.355-356

1999

Volltextzugriff (PDF)

Severe autosomal dominant retinitis pigmentosa caused by a novel rhodopsin mutation (Ter349Glu). Mutations in brief no. 208. Online

Human mutation, 1999, Vol.13 (1), p.83-83

1999

Volltextzugriff (PDF)

Management of strabismus due to orbital myositis

Eye (London), 1995-01, Vol.9 (5), p.558-563

1995

Volltextzugriff (PDF)

Epithelial debridement for secondary hyperopia following myopic excimer laser photorefractive keratectomy

Journal of cataract and refractive surgery, 1998-01, Vol.24 (1), p.31-34

1998

Volltextzugriff (PDF)

Further refinement of the Usher 2A locus at 1q41

Journal of medical genetics, 1998-09, Vol.35 (9), p.773-774

1998

Volltextzugriff (PDF)

An Analysis of ABCR Mutations in British Patients with Recessive Retinal Dystrophies

Investigative ophthalmology & visual science, 2000-01, Vol.41 (1), p.16-19

2000

Volltextzugriff (PDF)

Spectrum of Mutations in USH2A in British Patients with Usher Syndrome Type II

Experimental eye research, 2001-05, Vol.72 (5), p.503-509

2001

Volltextzugriff (PDF)

Clinical features of codon 172 RDS macular dystrophy: similar phenotype in 12 families

Archives of ophthalmology (1960), 1999-10, Vol.117 (10), p.1373

1999

Volltextzugriff (PDF)

NRL S50T mutation and the importance of 'founder effects' in inherited retinal dystrophies

European journal of human genetics : EJHG, 2000-10, Vol.8 (10), p.783-787

2000

Volltextzugriff (PDF)

Refinement of the Locus for Autosomal Recessive Retinitis Pigmentosa (RP25) Linked to Chromosome 6q in a Family of Pakistani Origin

American journal of human genetics, 1999-08, Vol.65 (2), p.571-574

1999

Volltextzugriff (PDF)

1 – 25 von 97

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(73)
Mit Volltextzugriff
(86)

Publikationsform

3 weitere anzeigen...

Weniger anzeigen...

Sprache

Englisch
(85)
Französisch
(11)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Molecular genetics and prospects for therapy of the inherited retinal dystrophies

Analysis of predictors of success in the MRCP (UK) PACES examination in candidates attending a revision course

Reduction in intraocular pressure after excimer laser photorefractive keratectomy : Correlation with pretreatment myopia

A Mutation in Guanylate Cyclase Activator 1A (GUCA1A) in an Autosomal Dominant Cone Dystrophy Pedigree Mapping to a New Locus on Chromosome 6p21.1

Valsalva retinopathy presenting with subhyaloid haemorrhage

Phenotype of autosomal recessive congenital microphthalmia mapping to chromosome 14q32

Genetic analysis of the guanylate cyclase activator 1B (GUCA1B) gene in patients with autosomal dominant retinal dystrophies

A Locus for Autosomal Recessive Congenital Microphthalmia Maps to Chromosome 14q32

Founder Effect, Seen in the British Population, of the 172 Peripherin/RDS Mutation—and Further Refinement of Genetic Positioning of the Peripherin/RDS Gene

Importance of the autosomal recessive retinitis pigmentosa locus on 1q31-q32.1 (RP12) and mutation analysis of the candidate gene RGS16 (RGS-r)

The management of dislocated lens material after phacoemulsification

Lamellar keratoplasty in the management of inflammatory corneal ulceration and perforation

Results of Excimer Laser Retreatment of Residual Myopia after Previous Photorefractive Keratectomy

Astigmatism Induced by Spherical Photorefractive Keratectomy Corrections

A New Locus for Autosomal Recessive RP (RP29) Mapping to Chromosome 4q32-q34 in a Pakistani Family

A mutation in NRL is associated with autosomal dominant retinitis pigmentosa

Severe autosomal dominant retinitis pigmentosa caused by a novel rhodopsin mutation (Ter349Glu). Mutations in brief no. 208. Online

Management of strabismus due to orbital myositis

Epithelial debridement for secondary hyperopia following myopic excimer laser photorefractive keratectomy

Further refinement of the Usher 2A locus at 1q41

An Analysis of ABCR Mutations in British Patients with Recessive Retinal Dystrophies

Spectrum of Mutations in USH2A in British Patients with Usher Syndrome Type II

Clinical features of codon 172 RDS macular dystrophy: similar phenotype in 12 families

NRL S50T mutation and the importance of 'founder effects' in inherited retinal dystrophies

Refinement of the Locus for Autosomal Recessive Retinitis Pigmentosa (RP25) Linked to Chromosome 6q in a Family of Pakistani Origin

Suchergebnisse filtern