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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 5

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164 results

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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
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
CHARGE syndrome: a recurrent hotspot of mutations in CHD7 IVS25 analyzed by bioinformatic tools and minigene assays.
Legendre M, Rodriguez-Ballesteros M, Rossi M, Abadie V, Amiel J, Revencu N, Blanchet P, Brioude F, Delrue MA, Doubaj Y, Sefiani A, Francannet C, Holder-Espinasse M, Jouk PS, Julia S, Melki J, Mur S, Naudion S, Fabre-Teste J, Busa T, Stamm S, Lyonnet S, Attie-Bitach T, Kitzis A, Gilbert-Dussardier B, Bilan F. Legendre M, et al. Among authors: sefiani a. Eur J Hum Genet. 2018 Feb;26(2):287-292. doi: 10.1038/s41431-017-0007-0. Epub 2017 Dec 18. Eur J Hum Genet. 2018. PMID: 29255276 Free PMC article.
164 results