Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

218 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
High incidence of the R276X SALL1 mutation in sporadic but not familial Townes-Brocks syndrome and report of the first familial case.
Kohlhase J, Liebers M, Backe J, Baumann-Müller A, Bembea M, Destrée A, Gattas M, Grüssner S, Müller T, Mortier G, Skrypnyk C, Yano S, Wirbelauer J, Michaelis RC. Kohlhase J, et al. Among authors: bembea m. J Med Genet. 2003 Nov;40(11):e127. doi: 10.1136/jmg.40.11.e127. J Med Genet. 2003. PMID: 14627694 Free PMC article. No abstract available.
Fanconi anemia with cleft palate.
Jurca A, Kinga K, Bembea M, Gug C, Jurca C. Jurca A, et al. Among authors: bembea m. Rev Med Chir Soc Med Nat Iasi. 2014 Oct-Dec;118(4):1074-7. Rev Med Chir Soc Med Nat Iasi. 2014. PMID: 25581972
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: bembea m. Genes (Basel). 2021 Oct 23;12(11):1674. doi: 10.3390/genes12111674. Genes (Basel). 2021. PMID: 34828280 Free PMC article. Review.
Clinical and genetic diversity of congenital hyperammonemia.
Jurcă AD, Jurcă MC, Bembea M, Kozma K, Budişteanu M, Gug C. Jurcă AD, et al. Among authors: bembea m. Rom J Morphol Embryol. 2018;59(3):945-948. Rom J Morphol Embryol. 2018. PMID: 30534838 Free article.
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: bembea m. 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: bembea m. Rom J Morphol Embryol. 2017;58(4):1531-1534. Rom J Morphol Embryol. 2017. PMID: 29556653 Free article.
218 results