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 Custom Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2010 1
2011 1
2018 2
2020 1
2021 2
2022 2
2023 1
2024 0

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

8 results

Results by year

Filters applied: . Clear all
Page 1
A COVID-19 family cluster with retinitis pigmentosa and hypogammaglobulinemia.
Alshukairi AN, Aldabbagh YA, Sayes NM, Al Gethamy MM, Alghamdi MG, Rahbeeni ZA, Dada A. Alshukairi AN, et al. Among authors: rahbeeni za. Ann Thorac Med. 2022 Jan-Mar;17(1):66-69. doi: 10.4103/atm.atm_520_21. Epub 2022 Jan 14. Ann Thorac Med. 2022. PMID: 35198051 Free PMC article.
Aortic calcification in Gaucher disease: a case report.
Alsahli S, Bubshait DK, Rahbeeni ZA, Alfadhel M. Alsahli S, et al. Among authors: rahbeeni za. Appl Clin Genet. 2018 Oct 17;11:107-110. doi: 10.2147/TACG.S180995. eCollection 2018. Appl Clin Genet. 2018. PMID: 30410382 Free PMC article.
Further delineation of Temtamy syndrome of corpus callosum and ocular abnormalities.
Alrakaf L, Al-Owain MA, Busehail M, Alotaibi MA, Monies D, Aldhalaan HM, Alhashem A, Al-Hassnan ZN, Rahbeeni ZA, Murshedi FA, Ani NA, Al-Maawali A, Ibrahim NA, Abdulwahab FM, Alsagob M, Hashem MO, Ramadan W, Abouelhoda M, Meyer BF, Kaya N, Maddirevula S, Alkuraya FS. Alrakaf L, et al. Among authors: rahbeeni za. Am J Med Genet A. 2018 Mar;176(3):715-721. doi: 10.1002/ajmg.a.38615. Epub 2018 Jan 31. Am J Med Genet A. 2018. PMID: 29383837
The clinical utility of rapid exome sequencing in a consanguineous population.
Monies D, Goljan E; Rapid Exome Consortium; Assoum M, Albreacan M, Binhumaid F, Subhani S, Boureggah A, Hashem M, Abdulwahab F, Abuyousef O, Temsah MH, Alsohime F, Kelaher J, Abouelhoda M, Meyer BF, Alkuraya FS. Monies D, et al. Genome Med. 2023 Jun 21;15(1):44. doi: 10.1186/s13073-023-01192-5. Genome Med. 2023. PMID: 37344829 Free PMC article.
Chromosome 16p13.3 Contiguous Gene Deletion Syndrome including the SLX4, DNASE1, TRAP1, and CREBBP Genes Presenting as a Relatively Mild Rubinstein-Taybi Syndrome Phenotype: A Case Report of a Saudi Boy.
Al-Qattan MM, Rahbeeni ZA, Al-Hassnan ZN, Jarman A, Rafique A, Mahabbat N, Alsufayan FAS. Al-Qattan MM, et al. Among authors: rahbeeni za. Case Rep Genet. 2020 Jan 9;2020:6143050. doi: 10.1155/2020/6143050. eCollection 2020. Case Rep Genet. 2020. PMID: 32181026 Free PMC article.