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Novel mutations of the tyrosinase (TYR) gene in type I oculocutaneous albinism (OCA1).
Spritz RA, Oh J, Fukai K, Holmes SA, Ho L, Chitayat D, France TD, Musarella MA, Orlow SJ, Schnur RE, Weleber RG, Levin AV. Spritz RA, et al. Among authors: chitayat d. Hum Mutat. 1997;10(2):171-4. doi: 10.1002/(SICI)1098-1004(1997)10:2<171::AID-HUMU11>3.0.CO;2-X. Hum Mutat. 1997. PMID: 9259202 No abstract available.
Cerebroretinal microangiopathy with calcifications and cysts (CRMCC).
Briggs TA, Abdel-Salam GM, Balicki M, Baxter P, Bertini E, Bishop N, Browne BH, Chitayat D, Chong WK, Eid MM, Halliday W, Hughes I, Klusmann-Koy A, Kurian M, Nischal KK, Rice GI, Stephenson JB, Surtees R, Talbot JF, Tehrani NN, Tolmie JL, Toomes C, van der Knaap MS, Crow YJ. Briggs TA, et al. Among authors: chitayat d. Am J Med Genet A. 2008 Jan 15;146A(2):182-90. doi: 10.1002/ajmg.a.32080. Am J Med Genet A. 2008. PMID: 18076099
Fetal hepatic calcifications: prenatal diagnosis and outcome.
Simchen MJ, Toi A, Bona M, Alkazaleh F, Ryan G, Chitayat D. Simchen MJ, et al. Among authors: chitayat d. Am J Obstet Gynecol. 2002 Dec;187(6):1617-22. doi: 10.1067/mob.2002.127899. Am J Obstet Gynecol. 2002. PMID: 12501073
567 results