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The clinical spectrum of homozygous HOXA1 mutations.
Bosley TM, Alorainy IA, Salih MA, Aldhalaan HM, Abu-Amero KK, Oystreck DT, Tischfield MA, Engle EC, Erickson RP. Bosley TM, et al. Am J Med Genet A. 2008 May 15;146A(10):1235-40. doi: 10.1002/ajmg.a.32262. Am J Med Genet A. 2008. PMID: 18412118 Free PMC article.
Exceptions to the Valsalva doctrine.
Schutta HS, Abu-Amero KK, Bosley TM. Schutta HS, et al. Neurology. 2010 Jan 26;74(4):329-35. doi: 10.1212/WNL.0b013e3181cbcd84. Neurology. 2010. PMID: 20101039 Review.
Ophthalmologic abnormalities in a de novo terminal 6q deletion.
Abu-Amero KK, Hellani A, Salih MA, Al Hussain A, al Obailan M, Zidan G, Alorainy IA, Bosley TM. Abu-Amero KK, et al. Ophthalmic Genet. 2010 Mar;31(1):1-11. doi: 10.3109/13816810903312535. Ophthalmic Genet. 2010. PMID: 20141352
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