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One or more keywords matched the following items that are connected to Vahidnezhad, Hassan
Item TypeName
Academic Article Lipoid proteinosis: phenotypic heterogeneity in Iranian families with c.507delT mutation in ECM1.
Academic Article The Kindler Syndrome: A Spectrum of FERMT1 Mutations in Iranian Families.
Academic Article Whole Genome Linkage Analysis Followed by Whole Exome Sequencing Identifies Nicastrin (NCSTN) as a Causative Gene in a Multiplex Family with ?-Secretase Spectrum of Autoinflammatory Skin Phenotypes.
Academic Article KRT5 and KRT14 Mutations in Epidermolysis Bullosa Simplex with Phenotypic Heterogeneity, and Evidence of Semidominant Inheritance in a Multiplex Family.
Academic Article Dystrophic Epidermolysis Bullosa: COL7A1 Mutation Landscape in a Multi-Ethnic Cohort of 152 Extended Families with High Degree of Customary Consanguineous Marriages.
Academic Article Gene-Targeted Next-Generation Sequencing Identifies a Novel CLDN1 Mutation in a Consanguineous Family With NISCH Syndrome.
Academic Article Genome-wide single nucleotide polymorphism-based autozygosity mapping facilitates identification of mutations in consanguineous families with epidermolysis bullosa.
Academic Article Autosomal recessive congenital ichthyosis: Genomic landscape and phenotypic spectrum in a cohort of 125 consanguineous families.
Academic Article A CIB1 Splice-Site Founder Mutation in Families with Typical Epidermodysplasia Verruciformis.
Academic Article Infantile systemic hyalinosis in an Iranian family with a mutation in the CMG2/ANTXR2 gene.
Academic Article BMI1 and TWIST1 downregulated mRNA expression in basal cell carcinoma.
Concept Snail Family Transcription Factors
Academic Article Homozygous ITGA3 Missense Mutation in Adults in a Family with Syndromic Epidermolysis Bullosa (ILNEB) without Pulmonary Involvement.
Academic Article Homozygous MEFV Gene Variant and Pyrin-Associated Autoinflammation With Neutrophilic Dermatosis: A Family With a Novel Autosomal Recessive Mode of Inheritance.
Academic Article Recalcitrant Cutaneous Warts in a Family with Inherited ICOS Deficiency.
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