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A novel INDEL mutation in the EDA gene resulting in a distinct X- linked hypohidrotic ectodermal dysplasia phenotype in an Italian family.
Callea M, Nieminen P, Willoughby CE, Clarich G, Yavuz I, Vinciguerra A, Di Stazio M, Giglio S, Sani I, Maglione M, Pensiero S, Tadini G, Bellacchio E. Callea M, et al. Among authors: yavuz i. J Eur Acad Dermatol Venereol. 2016 Feb;30(2):341-3. doi: 10.1111/jdv.12747. Epub 2014 Sep 30. J Eur Acad Dermatol Venereol. 2016. PMID: 25266272 No abstract available.
Ear nose throat manifestations in hypoidrotic ectodermal dysplasia.
Callea M, Teggi R, Yavuz I, Tadini G, Priolo M, Crovella S, Clarich G, Grasso DL. Callea M, et al. Among authors: yavuz i. Int J Pediatr Otorhinolaryngol. 2013 Nov;77(11):1801-4. doi: 10.1016/j.ijporl.2013.09.004. Epub 2013 Sep 13. Int J Pediatr Otorhinolaryngol. 2013. PMID: 24080322 Review.
[Clinical and molecular study in a family with cleidocranial dysplasia].
Callea M, Fattori F, Bertini ES, Yavuz I, Bellacchio E, Avendaño A, Araque D, Lacruz-Rengel MA, Da Silva G, Cammarata-Scalisi F. Callea M, et al. Among authors: yavuz i. Arch Argent Pediatr. 2017 Dec 1;115(6):e440-e444. doi: 10.5546/aap.2017.e440. Arch Argent Pediatr. 2017. PMID: 29087131 Free article. Spanish.
181 results