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W H McLean

Showing results (31-40 of 76) with videos related to

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The British Journal of Ophthalmology|April 27, 2000
A novel keratin 12 mutation in a German kindred with Meesmann's corneal dystrophyL D Corden, O Swensson, B Swensson, et al.
Biochemical Society Transactions|April 1, 1990
Reduced secretion of specific proteins in dystrophic fibroblastsW H McLean, K Patel, A E Hughes, et al.
Human Molecular Genetics|January 1, 1994
The gene for Darier's disease maps between D12S78 and D12S79E Parfitt, S Burge, N Craddock, et al.
The British Journal of Dermatology|November 13, 2001
Keratin K6irs is specific to the inner root sheath of hair follicles in mice and humansR M Porter, L D Corden, D P Lunny, et al.
Genomics|March 3, 1999
Human periplakin: genomic organization in a clonally unstable region of chromosome 16p with an abundance of repetitive sequence elementsS Aho, K Rothenberger, E M Tan, et al.
The Journal of Investigative Dermatology|May 12, 2001
Novel keratin 17 mutations in pachyonychia congenita type 2F J Smith, C M Coleman, N M Bayoumy, et al.
Experimental Dermatology|December 22, 1999
Analysis of the desmoplakin gene reveals striking conservation with other members of the plakin family of cytolinkersK J Green, S G Guy, P B Cserhalmi-Friedman, et al.
Experimental Dermatology|May 8, 1999
Novel and recurrent mutations in keratin 10 causing bullous congenital ichthyosiform erythrodermaW H McLean, S M Morley, C Higgins, et al.
The British Journal of Dermatology|May 8, 1999
Ichthyosis bullosa of Siemens: report of a family with evidence of a keratin 2e mutation, and a review of the literatureT Basarab, F J Smith, V M Jolliffe, et al.
The Journal of Clinical Investigation|November 15, 1996
A homozygous nonsense mutation in the PLEC1 gene in patients with epidermolysis bullosa simplex with muscular dystrophyS Chavanas, L Pulkkinen, Y Gache, et al.
Pageof 8

Showing results (31-40 of 76) with videos related to

Sort By:
Pageof 8
The British Journal of Ophthalmology|April 27, 2000
A novel keratin 12 mutation in a German kindred with Meesmann's corneal dystrophyL D Corden, O Swensson, B Swensson, et al.
Biochemical Society Transactions|April 1, 1990
Reduced secretion of specific proteins in dystrophic fibroblastsW H McLean, K Patel, A E Hughes, et al.
Human Molecular Genetics|January 1, 1994
The gene for Darier's disease maps between D12S78 and D12S79E Parfitt, S Burge, N Craddock, et al.
The British Journal of Dermatology|November 13, 2001
Keratin K6irs is specific to the inner root sheath of hair follicles in mice and humansR M Porter, L D Corden, D P Lunny, et al.
Genomics|March 3, 1999
Human periplakin: genomic organization in a clonally unstable region of chromosome 16p with an abundance of repetitive sequence elementsS Aho, K Rothenberger, E M Tan, et al.
The Journal of Investigative Dermatology|May 12, 2001
Novel keratin 17 mutations in pachyonychia congenita type 2F J Smith, C M Coleman, N M Bayoumy, et al.
Experimental Dermatology|December 22, 1999
Analysis of the desmoplakin gene reveals striking conservation with other members of the plakin family of cytolinkersK J Green, S G Guy, P B Cserhalmi-Friedman, et al.
Experimental Dermatology|May 8, 1999
Novel and recurrent mutations in keratin 10 causing bullous congenital ichthyosiform erythrodermaW H McLean, S M Morley, C Higgins, et al.
The British Journal of Dermatology|May 8, 1999
Ichthyosis bullosa of Siemens: report of a family with evidence of a keratin 2e mutation, and a review of the literatureT Basarab, F J Smith, V M Jolliffe, et al.
The Journal of Clinical Investigation|November 15, 1996
A homozygous nonsense mutation in the PLEC1 gene in patients with epidermolysis bullosa simplex with muscular dystrophyS Chavanas, L Pulkkinen, Y Gache, et al.
Pageof 8