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Nature Genetics|August 1, 1994
Mutations in the rod domain of keratin 2e in patients with ichthyosis bullosa of SiemensJ A Rothnagel, H Traupe, S Wojcik, et al.Journal of Cancer Education : the Official Journal of the American Association for Cancer Education|October 2, 2014
Medical Advocacy and Supportive Environments for African-Americans Following Abnormal MammogramsYamile Molina, Bridgette H Hempstead, Jacci Thompson-Dodd, et al.Cultural Diversity & Ethnic Minority Psychology|May 24, 2016
Ethnic differences in social support after initial receipt of an abnormal mammogramYamile Molina, Sarah D Hohl, Michelle Nguyen, et al.The Journal of Investigative Dermatology|March 1, 1997
A novel dinucleotide mutation in keratin 10 in the annular epidermolytic ichthyosis variant of bullous congenital ichthyosiform erythrodermaG Y Joh, H Traupe, D Metze, et al.Human Molecular Genetics|December 1, 1993
A mutational hot spot in keratin 10 (KRT 10) in patients with epidermolytic hyperkeratosisJ A Rothnagel, M P Fisher, S M Axtell, et al.Science (New York, N.Y.)|January 27, 1995
Mutations of keratinocyte transglutaminase in lamellar ichthyosisM Huber, I Rettler, K Bernasconi, et al.Research Evaluation|March 7, 2022
Transdisciplinary research outcomes based on the Transdisciplinary Research on Energetics and Cancer II initiative experienceSarah D Hohl, Sarah Knerr, Sarah Gehlert, et al.Archives of Dermatological Research|January 1, 1995
Altered distribution of keratinization markers in epidermolytic hyperkeratosisA Ishida-Yamamoto, H Iizuka, M Manabe, et al.Prevention Science : the Official Journal of the Society for Prevention Research|March 23, 2023
Implementing Mailed Colorectal Cancer Fecal Screening Tests in Real-World Primary Care Settings: Promising Implementation Practices and Opportunities for ImprovementSarah D Hohl, Annette E Maxwell, Krishna P Sharma, et al.Nature Genetics|December 8, 1998
Mutations in the human connexin gene GJB3 cause erythrokeratodermia variabilisG Richard, L E Smith, R A Bailey, et al.Pageof 14