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

19 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Diagnostic Yield and Novel Candidate Genes by Exome Sequencing in 152 Consanguineous Families With Neurodevelopmental Disorders.
Reuter MS, Tawamie H, Buchert R, Hosny Gebril O, Froukh T, Thiel C, Uebe S, Ekici AB, Krumbiegel M, Zweier C, Hoyer J, Eberlein K, Bauer J, Scheller U, Strom TM, Hoffjan S, Abdelraouf ER, Meguid NA, Abboud A, Al Khateeb MA, Fakher M, Hamdan S, Ismael A, Muhammad S, Abdallah E, Sticht H, Wieczorek D, Reis A, Abou Jamra R. Reuter MS, et al. Among authors: abdelraouf er. JAMA Psychiatry. 2017 Mar 1;74(3):293-299. doi: 10.1001/jamapsychiatry.2016.3798. JAMA Psychiatry. 2017. PMID: 28097321
Prevalence of consanguineous marriages in South Sinai, Egypt.
Yamamah G, Abdel-Raouf E, Talaat A, Saad-Hussein A, Hamamy H, Meguid NA. Yamamah G, et al. J Biosoc Sci. 2013 Jan;45(1):31-9. doi: 10.1017/S002193201200020X. Epub 2012 May 14. J Biosoc Sci. 2013. PMID: 22583662
Prevalence and risk factors of disabilities among Egyptian preschool children: a community-based population study.
Metwally AM, Aboulghate A, Elshaarawy GA, Abdallah AM, Abdel Raouf ER, El-Din EMS, Khadr Z, El-Saied MM, Elabd MA, Nassar MS, Abouelnaga MW, Ashaat EA, El-Sonbaty MM, Badawy HY, Dewdar EM, Salama SI, Abdelrahman M, Abdelmohsen AM, Eldeeb SE, Naga MM, Elshamy NH, Shaaban FA, ElRifay AS. Metwally AM, et al. BMC Psychiatry. 2023 Sep 21;23(1):689. doi: 10.1186/s12888-023-05171-3. BMC Psychiatry. 2023. PMID: 37735643 Free PMC article.
Expansion of the phenotypic and mutational spectrum of Carpenter syndrome.
Khairat R, Elhossini R, Sobreira N, Wohler E, Otaify G, Mohamed AM, Abdel Raouf ER, Sayed I, Aglan M, Ismail S, Temtamy SA. Khairat R, et al. Eur J Med Genet. 2022 Jan;65(1):104377. doi: 10.1016/j.ejmg.2021.104377. Epub 2021 Nov 5. Eur J Med Genet. 2022. PMID: 34748996
Johnson-McMillin Microtia Syndrome: New Additional Family.
Abdel-Meguid N, Gebril OH, Abdelraouf ER, Shafie MA, Bahgat M. Abdel-Meguid N, et al. Among authors: abdelraouf er. J Family Med Prim Care. 2014 Jul;3(3):275-8. doi: 10.4103/2249-4863.141639. J Family Med Prim Care. 2014. PMID: 25374870 Free PMC article.
19 results