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One or more keywords matched the following properties of Vahidnezhad, Hassan
keywords Mendelian Disorders
One or more keywords matched the following items that are connected to Vahidnezhad, Hassan
Item TypeName
Concept Blister
Concept Breast Neoplasms
Concept Carcinoma, Basal Cell
Concept Eczema
Concept Epidermodysplasia Verruciformis
Concept Epidermolysis Bullosa
Concept Ichthyosis
Concept Keratosis
Concept Lipoma
Concept Melanoma
Concept Musculoskeletal Abnormalities
Concept Mycoses
Concept Nevus
Concept Periodontal Diseases
Concept Photosensitivity Disorders
Concept Pseudoxanthoma Elasticum
Concept Skin Diseases
Concept Skin Diseases, Vesiculobullous
Concept Skin Neoplasms
Concept Syndrome
Concept Epidermolysis Bullosa Dystrophica
Concept Epidermolysis Bullosa, Junctional
Concept Epidermolysis Bullosa Simplex
Concept Skin Diseases, Vascular
Concept Ichthyosis, Lamellar
Concept Vascular Malformations
Concept Hyalinosis, Systemic
Concept Vascular Calcification
Academic Article Phenotypic Spectrum of Epidermolysis Bullosa: The Paradigm of Syndromic Versus Non-Syndromic Skin Fragility Disorders.
Academic Article Using immunofluorescence (antigen) mapping in the diagnosis and classification of epidermolysis bullosa: a first report from Iran.
Academic Article Genomics-based treatment in a patient with two overlapping heritable skin disorders: Epidermolysis bullosa and acrodermatitis enteropathica.
Academic Article Molecular Genetics of Keratinization Disorders - What's New About Ichthyosis.
Academic Article Research Techniques Made Simple: Whole-Transcriptome Sequencing by RNA-Seq for Diagnosis of Monogenic Disorders.
Academic Article Whole-Transcriptome Analysis by RNA Sequencing for Genetic Diagnosis of Mendelian Skin Disorders in the Context of Consanguinity.
Academic Article The utility of dermal fibroblasts in treatment of skin disorders: A paradigm of recessive dystrophic epidermolysis bullosa.
Academic Article Genetic heterogeneity of heritable ectopic mineralization disorders in a large international cohort.
Academic Article ENPP1 variants in patients with GACI and PXE expand the clinical and genetic heterogeneity of heritable disorders of ectopic calcification.
Search Criteria
  • Mendelian
  • Disorders