The EEC syndrome and SHFM: report of two cases and mutation analysis of

Autor: Ergin, H, Semerci, CN, Karakus, YT, Scheffer, H, Ergin, S, Koltuksuz, U, Meijer, R, Satiroglu-Tufan, NL

The p63 gene is a transcription factor and a member of the p53 family. Heterozygote mutation of the p63 gene is suggested in a number of human syndromes including limb development and/or ectodermal dysplasia. The EEC syndrome, consisting of ectrodact

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3566::9d1eb052430f6e5c1511bf6fe2c18e02
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/12915

Enteric duplication cyst located at the posterior tongue: a rare case report and review of the literature.

Autor: Savran B; Department of Pediatric Surgery, Faculty of Medicine, Dumlupinar University, 43000 Kutahya, Turkey., Kucur C; Department of Otolaryngology, Faculty of Medicine, Dumlupinar University, 43000 Kutahya, Turkey., Kocak C; Department of Pathology, Faculty of Medicine, Dumlupinar University, 43000 Kutahya, Turkey., Ozbay I; Department of Otolaryngology, Faculty of Medicine, Dumlupinar University, 43000 Kutahya, Turkey., Metineren MH; Department of Pathology, Faculty of Medicine, Dumlupinar University, 43000 Kutahya, Turkey., Karakus YT; Department of Pediatrics, Faculty of Medicine, Dumlupinar University, 43000 Kutahya, Turkey.

Publikováno v: Case reports in otolaryngology [Case Rep Otolaryngol] 2015; Vol. 2015, pp. 951878. Date of Electronic Publication: 2015 Feb 23.

Frequency of hematological findings associated with severe plasma vitamin B12 deficiency in infants and adolescents.

Autor: Atay E, Akin M, Ozhan B, Osman O, Karakus YT, Erdogan F

Publikováno v: Clinical laboratory [Clin Lab] 2014; Vol. 60 (4), pp. 659-62.