Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Alopecia and TGM1[original query] |
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Novel transglutaminase-1 mutations and genotype-phenotype investigations of 104 patients with autosomal recessive congenital ichthyosis in the USA. Journal of medical genetics 2009 Feb 46 (2): 103-11. Farasat S, Wei M-H, Herman M, Liewehr D J, Steinberg S M, Bale S J, Fleckman P, Toro J |
The Genomic and Phenotypic Landscape of Ichthyosis: An Analysis of 1000 Kindreds. JAMA dermatology 2021 12 158 (1): 16-25. Sun Qisi, Burgren Nareh M, Cheraghlou Shayan, Paller Amy S, Larralde Margarita, Bercovitch Lionel, Levinsohn Jonathan, Ren Ivy, Hu Rong Hua, Zhou Jing, Zaki Theodore, Fan Ryan, Tian Charlie, Saraceni Corey, Nelson-Williams Carol J, Loring Erin, Craiglow Brittany G, Milstone Leonard M, Lifton Richard P, Boyden Lynn M, Choate Keith |
Cross-sectional study on autosomal recessive congenital ichthyoses: association of genotype with disease severity, phenotypic and ultrastructural features in 74 Italian patients. Dermatology (Basel, Switzerland) 2024 4 . Andrea Diociaiuti, Marialuisa Corbeddu, Sabrina Rossi, Elisa Pisaneschi, Claudia Cesario, Angelo Giuseppe Condorelli, Tonia Samela, Simona Giancristoforo, Adriano Angioni, Giovanna Zambruno, Antonio Novelli, Rita Alaggio, Damiano Abeni, May El Hach |
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- Page last updated:Apr 16, 2024
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