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

Year Number of Results
1992 1
1993 1
1994 3
1995 1
1996 2
1997 3
1998 2
1999 1
2000 1
2002 2
2003 1
2004 2
2006 13
2007 3
2008 2
2009 1
2010 2
2012 1
2013 2
2014 1
2016 3
2017 3
2018 1
2019 2
2021 1
2022 3
2023 2

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55 results

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Page 1
Exome Sequencing Reveals Novel TTN Variants in Saudi Patients with Congenital Titinopathies.
Salih MA, Hamad MH, Savarese M, Alorainy IA, Al-Jarallah AS, Alkhalidi H, AlQudairy H, Albader A, Alotaibi AJ, Alsagob M, Al-Bakheet A, Colak D, Udd B, Kaya N. Salih MA, et al. Among authors: al jarallah as. Genet Test Mol Biomarkers. 2021 Dec;25(12):757-764. doi: 10.1089/gtmb.2021.0085. Genet Test Mol Biomarkers. 2021. PMID: 34918981
Cardiac diseases as a risk factor for stroke in Saudi children.
Salih MA, Al-Jarallah AS, Abdel-Gader AG, Al-Jarallah AA, Al-Saadi MM, Kentab AY, Alorainy IA, Hassan HH. Salih MA, et al. Among authors: al jarallah aa, al jarallah as. Saudi Med J. 2006 Mar;27 Suppl 1:S61-8. Saudi Med J. 2006. PMID: 16532133
Efficient identification of novel mutations in patients with limb girdle muscular dystrophy.
Boyden SE, Salih MA, Duncan AR, White AJ, Estrella EA, Burgess SL, Seidahmed MZ, Al-Jarallah AS, Alkhalidi HM, Al-Maneea WM, Bennett RR, Alshemmari SH, Kunkel LM, Kang PB. Boyden SE, et al. Among authors: al jarallah as. Neurogenetics. 2010 Oct;11(4):449-55. doi: 10.1007/s10048-010-0250-9. Epub 2010 Jul 13. Neurogenetics. 2010. PMID: 20623375 Free PMC article.
55 results