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Maureen Laidlaw

Research Profile

Chemicals & Drugs

Disorders

Anatomy

Procedures

Living Beings

Physiology

Genes & Molecular Sequences

Dominant Genes

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Publications

TOP 3
Allan J Richards; Maureen Laidlaw; Sarah P Meredith; Pallavi Shankar; Arabella V Poulson; John D Scott; Martin P Snead
Missense and silent mutations in COL2A1 result in Stickler syndrome but via different molecular mechanisms.
Alan Ang; Tsiang Ung; Narman Puvanachandra; Louise Wilson; Frances Howard; Michael Ryalls; Allan Richards; Sarah P Meredith; Maureen Laidlaw; Arabella V Poulson; John Scott; Martin Snead
Vitreous phenotype: a key diagnostic sign in Stickler syndrome types 1 and 2 complicated by double heterozygosity.
Allan J Richards; Maureen Laidlaw; Joanne Whittaker; Becky Treacy; Harjeet Rai; P W P Bearcroft; David M Baguley; Arabella V Poulson; Alan Ang; John D Scott; Martin P Snead
High efficiency of mutation detection in type 1 stickler syndrome using a two-stage approach: vitreoretinal assessment coupled with exon sequencing for screening COL2A1.

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All Publications

2007: Allan J Richards; Maureen Laidlaw; Sarah P Meredith; Pallavi Shankar; Arabella V Poulson; John D Scott; Martin P Snead
Missense and silent mutations in COL2A1 result in Stickler syndrome but via different molecular mechanisms.
Human mutation 2007;28(6):639.
2007: Alan Ang; Tsiang Ung; Narman Puvanachandra; Louise Wilson; Frances Howard; Michael Ryalls; Allan Richards; Sarah P Meredith; Maureen Laidlaw; Arabella V Poulson; John Scott; Martin Snead
Vitreous phenotype: a key diagnostic sign in Stickler syndrome types 1 and 2 complicated by double heterozygosity.
American journal of medical genetics. Part A 2007;143(6):604-7.
2006: Allan J Richards; Maureen Laidlaw; Joanne Whittaker; Becky Treacy; Harjeet Rai; P W P Bearcroft; David M Baguley; Arabella V Poulson; Alan Ang; John D Scott; Martin P Snead
High efficiency of mutation detection in type 1 stickler syndrome using a two-stage approach: vitreoretinal assessment coupled with exon sequencing for screening COL2A1.
Human mutation 2006;27(7):696-704.

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