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Journal Article
Boppudi, S., Boegershausen, N., Hove, H. B., Percin, E. F., Aslan, D., Dvorsky, R., Kayhan, G., Li, Y., Cursiefen, C., Tantcheva-Poor, I., Toft, P. B., Bartsch, O., Lissewski, C., Wieland, I., Jakubiczka, S., Wollnik, B., Ahmadian, M. R., Heindl, L. M. and Zenker, M. (2016). Specific mosaic KRAS mutations affecting codon 146 cause oculoectodermal syndrome and encephalocraniocutaneous lipomatosis. Clin. Genet., 90 (4). S. 334 - 343. HOBOKEN: WILEY-BLACKWELL. ISSN 1399-0004
Budisteanu, M., Boegershausen, N., Papuc, S. M., Moosa, S., Thoenes, M., Riga, D., Arghir, A. and Wollnik, B. (2018). FLOATING-HARBOR SYNDROME: PRESENTATION OF THE FIRST ROMANIAN PATIENT WITH A SRCAP MUTATION AND REVIEW OF THE LITERATURE. Balk. J. Med. Gen., 21 (1). S. 83 - 87. SKOPJE: MACEDONIAN ACAD SCIENCES ARTS. ISSN 1311-0160