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RHBDF2 Mutations Are Associated with Tylosis, a Familial Esophageal Cancer Syndrome

American journal of human genetics, 2012-02, Vol.90 (2), p.340-346

2012

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Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrix

Nature genetics, 1997-08, Vol.16 (4), p.372-374

1997

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Recessive mutation in desmoplakin disrupts desmoplakin-intermediate filament interactions and causes dilated cardiomyopathy, woolly hair and keratoderma

Human molecular genetics, 2000-11, Vol.9 (18), p.2761-2766

2000

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Mal de Meleda (MDM) caused by mutations in the gene for SLURP-1 in patients from Germany, Turkey, Palestine, and the United Arab Emirates

Human genetics, 2003, Vol.112 (1), p.50-56

2003

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The use of Reflectance Confocal Microscopy to diagnose Basal Cell Carcinoma in the United Kingdom: A Prospective Observational Trial at a Single Centre

British journal of dermatology (1951), 2024-09

2024

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The use of Reflectance Confocal Microscopy to diagnose Malignant Melanoma and Lentigo Maligna in the United Kingdom: A Prospective Observational Trial at a Single Centre

British journal of dermatology (1951), 2024-09

2024

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Spectrum of dominant mutations in the desmosomal cadherin desmoglein 1, causing the skin disease striate palmoplantar keratoderma

European journal of human genetics : EJHG, 2001-03, Vol.9 (3), p.197-203

2001

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Characterization of Paraneoplastic Pemphigus Autoantigens by Immunoblot Analysis

Journal of investigative dermatology, 1995-05, Vol.104 (5), p.829-834

1995

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Connexin mutations associated with palmoplantar keratoderma and profound deafness in a single family

European journal of human genetics : EJHG, 2000-02, Vol.8 (2), p.141-144

2000

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An unusual presentation of a common disease

Dermatology online journal, 2008-03, Vol.14 (3), p.4-4

2008

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A new mutation in the type II hair cortex keratin hHb1 involved in the inherited hair disorder monilethrix

Human genetics, 1997-12, Vol.101 (2), p.165-169

1997

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The Gene for Hypotrichosis of Marie Unna Maps between D8S258 and D8S298: Exclusion of the hr Gene by cDNA and Genomic Sequencing

American journal of human genetics, 1999-08, Vol.65 (2), p.413-419

1999

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Working toward a model of demonstrated value in predicting and developing leadership success

Advances in Global Leadership, 2011, Vol.6, p.217-242

2011

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Total Quality Management Now Applies to Managing Talent

The Journal for quality and participation, 2008-07, Vol.31 (2), p.15

Stevens, Howard P

2008

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N-Terminal Deletion in a Desmosomal Cadherin Causes the Autosomal Dominant Skin Disease Striate Palmoplantar Keratoderma

Human molecular genetics, 1999-06, Vol.8 (6), p.971-976

1999

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The palmoplantar keratodermas: much more than palms and soles

Molecular Medicine Today, 1999-03, Vol.5 (3), p.107-113

1999

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A Gene for an Autosomal Dominant Scleroatrophic Syndrome Predisposing to Skin Cancer (Huriez Syndrome) Maps to Chromosome 4q23

American journal of human genetics, 2000, Vol.66 (1), p.326-330

2000

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A Test Comparison of SAC and Non-SAC Pb-Free Solders

Circuits Assembly, 2007-12, Vol.18 (12), p.24

Stevens, Howard P

2007

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Localisation of a gene for Papillon-Lefèvre syndrome to chromosome 11q14-q21 by homozygosity mapping

Human genetics, 1997-12, Vol.101 (3), p.376-382

1997

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Connexin mutations associated with palmoplantar keratoderma and profound deafness in a single family

European journal of human genetics : EJHG, 2000-06, Vol.8 (6), p.468-468

2000

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Close Mapping of the Focal Non-Epidermolytic Palmoplantar Keratoderma (PPK) Locus Associated with Oesophageal Cancer (TOC)

Human molecular genetics, 1996-06, Vol.5 (6), p.857-860

1996

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Linkage of Monilethrix to the Trichocyte and Epithelial Keratin Gene Cluster on 12q11-q13

Journal of investigative dermatology, 1996-04, Vol.106 (4), p.795-797

1996

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Linkage of an American pedigree with palmoplantar keratoderma and malignancy (palmoplantar ectodermal dysplasia type III) to 17q24. Literature survey and proposed updated classification of the keratodermas

Archives of dermatology (1960), 1996-06, Vol.132 (6), p.640

1996

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Erratum: Connexin mutations associated with palmoplantar keratoderma and profound deafness in a single family

European journal of human genetics : EJHG, 2000-06, Vol.8 (6), p.468-468

2000

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Genetic linkage studies in non-epidermolytic palmoplantar keratoderma: evidence for heterogeneity

Human molecular genetics, 1995-06, Vol.4 (6), p.1021-1025

1995

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RHBDF2 Mutations Are Associated with Tylosis, a Familial Esophageal Cancer Syndrome

Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrix

Recessive mutation in desmoplakin disrupts desmoplakin-intermediate filament interactions and causes dilated cardiomyopathy, woolly hair and keratoderma

Mal de Meleda (MDM) caused by mutations in the gene for SLURP-1 in patients from Germany, Turkey, Palestine, and the United Arab Emirates

The use of Reflectance Confocal Microscopy to diagnose Basal Cell Carcinoma in the United Kingdom: A Prospective Observational Trial at a Single Centre

The use of Reflectance Confocal Microscopy to diagnose Malignant Melanoma and Lentigo Maligna in the United Kingdom: A Prospective Observational Trial at a Single Centre

Spectrum of dominant mutations in the desmosomal cadherin desmoglein 1, causing the skin disease striate palmoplantar keratoderma

Characterization of Paraneoplastic Pemphigus Autoantigens by Immunoblot Analysis

Connexin mutations associated with palmoplantar keratoderma and profound deafness in a single family

An unusual presentation of a common disease

A new mutation in the type II hair cortex keratin hHb1 involved in the inherited hair disorder monilethrix

The Gene for Hypotrichosis of Marie Unna Maps between D8S258 and D8S298: Exclusion of the hr Gene by cDNA and Genomic Sequencing

Working toward a model of demonstrated value in predicting and developing leadership success

Total Quality Management Now Applies to Managing Talent

N-Terminal Deletion in a Desmosomal Cadherin Causes the Autosomal Dominant Skin Disease Striate Palmoplantar Keratoderma

The palmoplantar keratodermas: much more than palms and soles

A Gene for an Autosomal Dominant Scleroatrophic Syndrome Predisposing to Skin Cancer (Huriez Syndrome) Maps to Chromosome 4q23

A Test Comparison of SAC and Non-SAC Pb-Free Solders

Localisation of a gene for Papillon-Lefèvre syndrome to chromosome 11q14-q21 by homozygosity mapping

Connexin mutations associated with palmoplantar keratoderma and profound deafness in a single family

Close Mapping of the Focal Non-Epidermolytic Palmoplantar Keratoderma (PPK) Locus Associated with Oesophageal Cancer (TOC)

Linkage of Monilethrix to the Trichocyte and Epithelial Keratin Gene Cluster on 12q11-q13

Linkage of an American pedigree with palmoplantar keratoderma and malignancy (palmoplantar ectodermal dysplasia type III) to 17q24. Literature survey and proposed updated classification of the keratodermas

Erratum: Connexin mutations associated with palmoplantar keratoderma and profound deafness in a single family

Genetic linkage studies in non-epidermolytic palmoplantar keratoderma: evidence for heterogeneity

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