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Publications by Cathy A Stevens

Epidermolysis Bullosa With Congenital Pyloric Atresia: Novel Mutations in the Β4 Integrin Gene (ITGB4) and Genotype/Phenotype Correlations

Pediatric Research

English

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Epidermolysis Bullosa Simplex Associated With Pyloric Atresia Is a Novel Clinical Subtype Caused by Mutations in the Plectin Gene (PLEC1)

Journal of Molecular Diagnostics

Forensic Medicine

Molecular Medicine

English

Prenatal Diagnosis of Junctional Epidermolysis Bullosa Associated With Pyloric Atresia.

Journal of Medical Genetics

English

Genotype–Phenotype Correlation in Chinese Patients With Dystrophic Epidermolysis Bullosa Pruriginosa

Acta Dermato-Venereologica

English

Management of Patients With Congenital Epidermolysis Bullosa

Vestnik dermatologii i venerologii

English

Novel Genotype-Phenotype and MRI Correlations in a Large Cohort of Patients With SPG7 Mutations

Neurology: Genetics

English

Genotype-Phenotype Correlations in PCD Patients Carrying DNAH5 Mutations

Respiratory Medicine

English

Gene Therapy for Epidermolysis Bullosa

Journal of Investigative Dermatology

Molecular Biology

English

Exclusion of Linkage Between the Collagenase Gene and Generalized Recessive Dystrophic Epidermolysis Bullosa Phenotype.

Journal of Clinical Investigation

English

Known and Novel Mutations Responsible for Epidermolysis Bullosa Simplex Cases in a Chinese Population

Experimental and Therapeutic Medicine

Cancer Research

English