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Greig Cephalopolysyndactyly Contiguous Gene Syndrome: Case Report and Literature Review.
Kozma K, Bembea M, Jurca CM, Ioana M, Streață I, Şoşoi SŞ, Pirvu A, Petchesi CD, Szilágyi A, Sava CN, Jurca A, Ujfalusi A, Szűcs Z, Szakszon K. Kozma K, et al. Among authors: petchesi cd. Genes (Basel). 2021 Oct 23;12(11):1674. doi: 10.3390/genes12111674. Genes (Basel). 2021. PMID: 34828280 Free PMC article. Review.
Anatomic variants in Dandy-Walker complex.
Jurcă MC, Kozma K, Petcheşi CD, Bembea M, Pop OL, MuŢiu G, Coroi MC, Jurcă AD, Dobjanschi L. Jurcă MC, et al. Among authors: petchesi cd. Rom J Morphol Embryol. 2017;58(3):1051-1055. Rom J Morphol Embryol. 2017. PMID: 29250689 Free article.
Morphological and genetic abnormalities in a Jacobsen syndrome.
Jurcă AD, Kozma K, Ioana M, Streaţă I, Petcheşi CD, Bembea M, Jurcă MC, Cuc EA, Vesa CM, Buhaş CL. Jurcă AD, et al. Among authors: petchesi cd. Rom J Morphol Embryol. 2017;58(4):1531-1534. Rom J Morphol Embryol. 2017. PMID: 29556653 Free article.
Empty sella associated with growth hormone deficiency and polydactyly.
Jurcă MC, Bembea M, Kozma K, Şandor MI, Negrean RA, Dobjanschi L, Cuc EA, Petcheşi CD, Jurcă AD. Jurcă MC, et al. Among authors: petchesi cd. Rom J Morphol Embryol. 2018;59(1):381-384. Rom J Morphol Embryol. 2018. PMID: 29940653 Free article.
Genetics of congenital solid tumors.
Jurcă MC, Ivaşcu ME, Jurcă AA, Kozma K, Magyar I, Şandor MI, Jurcă AD, Zaha DC, Albu CC, Pantiş C, Bembea M, Petcheşi CD. Jurcă MC, et al. Among authors: petchesi cd. Rom J Morphol Embryol. 2020 Oct-Dec;61(4):1039-1049. doi: 10.47162/RJME.61.4.06. Rom J Morphol Embryol. 2020. PMID: 34171053 Free PMC article.
12 results