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Vahidnezhad, Hassan
One or more keywords matched the following items that are connected to
Vahidnezhad, Hassan
Item Type
Name
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.
Search Criteria
Family