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Characterizing the morbid genome of ciliopathies.
Shaheen R, Szymanska K, Basu B, Patel N, Ewida N, Faqeih E, Al Hashem A, Derar N, Alsharif H, Aldahmesh MA, Alazami AM, Hashem M, Ibrahim N, Abdulwahab FM, Sonbul R, Alkuraya H, Alnemer M, Al Tala S, Al-Husain M, Morsy H, Seidahmed MZ, Meriki N, Al-Owain M, AlShahwan S, Tabarki B, Salih MA; Ciliopathy WorkingGroup; Faquih T, El-Kalioby M, Ueffing M, Boldt K, Logan CV, Parry DA, Al Tassan N, Monies D, Megarbane A, Abouelhoda M, Halees A, Johnson CA, Alkuraya FS. Shaheen R, et al. Among authors: salih ma. Genome Biol. 2016 Nov 28;17(1):242. doi: 10.1186/s13059-016-1099-5. Genome Biol. 2016. PMID: 27894351 Free PMC article.
Brain stem and cerebellar findings in Joubert syndrome.
Alorainy IA, Sabir S, Seidahmed MZ, Farooqu HA, Salih MA. Alorainy IA, et al. Among authors: salih ma. J Comput Assist Tomogr. 2006 Jan-Feb;30(1):116-21. doi: 10.1097/01.rct.0000191681.05473.13. J Comput Assist Tomogr. 2006. PMID: 16365585
Deletion of short arm of chromosome 3 in a Saudi girl.
Al Husain MA, Zaki OK, Salih MA. Al Husain MA, et al. Among authors: salih ma. Ann Saudi Med. 1996 Jul;16(4):455-7. doi: 10.5144/0256-4947.1996.455. Ann Saudi Med. 1996. PMID: 17372514 Free article. No abstract available.
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: salih ma. 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.
318 results