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

Year Number of Results
1993 1
1998 4
1999 2
2001 1
2002 2
2003 4
2004 4
2005 4
2006 1
2007 1
2008 5
2009 8
2010 5
2011 1
2012 3
2014 2
2015 2
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2018 2
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2020 2
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2024 0

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52 results

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Page 1
[Arterial tortuosity syndrome].
Meyer S, Faiyaz-Ul-Haque M, Zankl M, Sailer NL, Marx N, Limbach HG, Lindinger A. Meyer S, et al. Among authors: faiyaz ul haque m. Klin Padiatr. 2005 Jan-Feb;217(1):36-40. doi: 10.1055/s-2004-822635. Klin Padiatr. 2005. PMID: 15640971 Review. German.
Genetics of glucose-6-phosphate dehydrogenase deficiency in Saudi patients.
Faiyaz-Ul-Haque M, Zaidi SH, Hasanato RM, Al-Abdullatif A, Cluntun A, Teresita G, Toulimat M, Al-Nounou R, Al-Dayel F, Peltekova I, Bhuiyan JA. Faiyaz-Ul-Haque M, et al. Clin Genet. 2010 Jul;78(1):98-100. doi: 10.1111/j.1399-0004.2010.01377.x. Epub 2010 Mar 4. Clin Genet. 2010. PMID: 20236109 No abstract available.
Exome sequencing reveals MCM8 mutation underlies ovarian failure and chromosomal instability.
AlAsiri S, Basit S, Wood-Trageser MA, Yatsenko SA, Jeffries EP, Surti U, Ketterer DM, Afzal S, Ramzan K, Faiyaz-Ul Haque M, Jiang H, Trakselis MA, Rajkovic A. AlAsiri S, et al. Among authors: faiyaz ul haque m. J Clin Invest. 2015 Jan;125(1):258-62. doi: 10.1172/JCI78473. Epub 2014 Dec 1. J Clin Invest. 2015. PMID: 25437880 Free PMC article.
Autoimmune polyglandular syndrome type 1 in Saudi children.
Bin-Abbas BS, Faiyaz-Ul-Haque M, Al-Fares AH, Al-Gazlan SS, Bhuiyan JA, Al-Muhsen SZ. Bin-Abbas BS, et al. Among authors: faiyaz ul haque m. Saudi Med J. 2010 Jul;31(7):788-92. Saudi Med J. 2010. PMID: 20635013
Rett Syndrome, a Neurodevelopmental Disorder, Whole-Transcriptome, and Mitochondrial Genome Multiomics Analyses Identify Novel Variations and Disease Pathways.
Aldosary M, Al-Bakheet A, Al-Dhalaan H, Almass R, Alsagob M, Al-Younes B, AlQuait L, Mustafa OM, Bulbul M, Rahbeeni Z, Alfadhel M, Chedrawi A, Al-Hassnan Z, AlDosari M, Al-Zaidan H, Al-Muhaizea MA, AlSayed MD, Salih MA, AlShammari M, Faiyaz-Ul-Haque M, Chishti MA, Al-Harazi O, Al-Odaib A, Kaya N, Colak D. Aldosary M, et al. Among authors: faiyaz ul haque m. OMICS. 2020 Mar;24(3):160-171. doi: 10.1089/omi.2019.0192. Epub 2020 Feb 27. OMICS. 2020. PMID: 32105570
Spectrum of the KIT Gene Mutations in Gastrointestinal Stromal Tumors in Arab Patients.
Faiyaz-Ul-Haque M, Al-Dayel F, Tulba A, Abalkhail H, Alhussaini H, Memon M, Bazarbashi S, Amin T, Satti MB, Peltekova I, Nawaz Z, Zaidi SH. Faiyaz-Ul-Haque M, et al. Asian Pac J Cancer Prev. 2018 Oct 26;19(10):2905-2910. doi: 10.22034/APJCP.2018.19.10.2905. Asian Pac J Cancer Prev. 2018. PMID: 30362320 Free PMC article.
52 results