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
1988 2
1989 3
1991 1
1993 1
1994 1
1996 1
1998 2
1999 1
2000 3
2002 3
2003 1
2005 2
2006 3
2007 7
2008 5
2009 4
2010 11
2011 11
2012 15
2013 8
2014 13
2015 10
2016 14
2017 17
2018 12
2019 3
2020 5
2021 8
2022 7
2023 6
2024 13

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

172 results

Results by year

Filters applied: . Clear all
Page 1
Autosomal dominant microtia.
Chafai Elalaoui S, Cherkaoui Jaouad I, Rifai L, Sefiani A. Chafai Elalaoui S, et al. Among authors: sefiani a. Eur J Med Genet. 2010 Mar-Apr;53(2):100-3. doi: 10.1016/j.ejmg.2010.02.002. Epub 2010 Feb 10. Eur J Med Genet. 2010. PMID: 20152949
Selective, Intrinsically Fluorescent Trk Modulating Probes.
Pewklang T, Thompson T, Sefiani A, Geoffroy CG, Kamkaew A, Burgess K. Pewklang T, et al. Among authors: sefiani a. ACS Chem Neurosci. 2024 Oct 2;15(20):3679-91. doi: 10.1021/acschemneuro.4c00290. Online ahead of print. ACS Chem Neurosci. 2024. PMID: 39356215 Free PMC article.
Non lethal Raine syndrome and differential diagnosis.
Elalaoui SC, Al-Sheqaih N, Ratbi I, Urquhart JE, O'Sullivan J, Bhaskar S, Williams SS, Elalloussi M, Lyahyai J, Sbihi L, Cherkaoui Jaouad I, Sbihi A, Newman WG, Sefiani A. Elalaoui SC, et al. Among authors: sefiani a. Eur J Med Genet. 2016 Nov;59(11):577-583. doi: 10.1016/j.ejmg.2016.09.018. Epub 2016 Sep 22. Eur J Med Genet. 2016. PMID: 27667191
Novel variant related to SATB2-associated syndrome.
Benyahya N, Amllal N, Elalaoui SC, El Alloussi M, Sefiani A, Lyahyai J. Benyahya N, et al. Among authors: sefiani a. Int J Dev Neurosci. 2024 Dec;84(8):1006-1009. doi: 10.1002/jdn.10379. Epub 2024 Sep 19. Int J Dev Neurosci. 2024. PMID: 39300047
172 results