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

Year Number of Results
2005 1
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2007 1
2008 1
2009 1
2010 5
2011 2
2012 8
2013 10
2014 6
2015 7
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2018 5
2019 8
2020 7
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2024 7

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102 results

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Page 1
Accelerating novel candidate gene discovery in neurogenetic disorders via whole-exome sequencing of prescreened multiplex consanguineous families.
Alazami AM, Patel N, Shamseldin HE, Anazi S, Al-Dosari MS, Alzahrani F, Hijazi H, Alshammari M, Aldahmesh MA, Salih MA, Faqeih E, Alhashem A, Bashiri FA, Al-Owain M, Kentab AY, Sogaty S, Al Tala S, Temsah MH, Tulbah M, Aljelaify RF, Alshahwan SA, Seidahmed MZ, Alhadid AA, Aldhalaan H, AlQallaf F, Kurdi W, Alfadhel M, Babay Z, Alsogheer M, Kaya N, Al-Hassnan ZN, Abdel-Salam GM, Al-Sannaa N, Al Mutairi F, El Khashab HY, Bohlega S, Jia X, Nguyen HC, Hammami R, Adly N, Mohamed JY, Abdulwahab F, Ibrahim N, Naim EA, Al-Younes B, Meyer BF, Hashem M, Shaheen R, Xiong Y, Abouelhoda M, Aldeeri AA, Monies DM, Alkuraya FS. Alazami AM, et al. Cell Rep. 2015 Jan 13;10(2):148-61. doi: 10.1016/j.celrep.2014.12.015. Epub 2014 Dec 31. Cell Rep. 2015. PMID: 25558065 Free article.
Hydrodynamic delivery.
Al-Dosari MS, Knapp JE, Liu D. Al-Dosari MS, et al. Adv Genet. 2005;54:65-82. doi: 10.1016/S0065-2660(05)54004-5. Adv Genet. 2005. PMID: 16096008 Review.
Novel CENPJ mutation causes Seckel syndrome.
Al-Dosari MS, Shaheen R, Colak D, Alkuraya FS. Al-Dosari MS, et al. J Med Genet. 2010 Jun;47(6):411-4. doi: 10.1136/jmg.2009.076646. J Med Genet. 2010. PMID: 20522431
102 results