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

Year Number of Results
2002 1
2003 2
2004 2
2005 4
2006 4
2007 2
2008 4
2009 2
2010 7
2011 5
2012 2
2013 1
2014 7
2015 4
2016 1
2017 2
2020 3
2022 1
2023 3
2024 1
2025 2
2026 0

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56 results

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Page 1
Molecular and clinical spectra of FBXL4 deficiency.
El-Hattab AW, Dai H, Almannai M, Wang J, Faqeih EA, Al Asmari A, Saleh MAM, Elamin MAO, Alfadhel M, Alkuraya FS, Hashem M, Aldosary MS, Almass R, Almutairi FB, Alsagob M, Al-Owain M, Al-Sharfa S, Al-Hassnan ZN, Rahbeeni Z, Al-Muhaizea MA, Makhseed N, Foskett GK, Stevenson DA, Gomez-Ospina N, Lee C, Boles RG, Schrier Vergano SA, Wortmann SB, Sperl W, Opladen T, Hoffmann GF, Hempel M, Prokisch H, Alhaddad B, Mayr JA, Chan W, Kaya N, Wong LC. El-Hattab AW, et al. Among authors: boles rg. Hum Mutat. 2017 Dec;38(12):1649-1659. doi: 10.1002/humu.23341. Epub 2017 Oct 6. Hum Mutat. 2017. PMID: 28940506 Review.
Ocular findings in geleophysic dysplasia.
Zhang X, Boles RG, Law SK, Lin M. Zhang X, et al. Among authors: boles rg. J AAPOS. 2004 Apr;8(2):198-200. doi: 10.1016/j.jaapos.2003.07.007. J AAPOS. 2004. PMID: 15088061 Review. No abstract available.
FGFR mutations and plagiocephaly.
Dhamcharee V, Boles RG. Dhamcharee V, et al. Among authors: boles rg. J Craniofac Surg. 2008 Jan;19(1):290-1. doi: 10.1097/SCS.0b013e31815ca1e6. J Craniofac Surg. 2008. PMID: 18216705
56 results