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Items: 3

1.

Brittle cornea syndrome ZNF469 mutation carrier phenotype and segregation analysis of rare ZNF469 variants in familial keratoconus.

Davidson AE, Borasio E, Liskova P, Khan AO, Hassan H, Cheetham ME, Plagnol V, Alkuraya FS, Tuft SJ, Hardcastle AJ.

Invest Ophthalmol Vis Sci. 2015 Jan 6;56(1):578-86. doi: 10.1167/iovs.14-15792.

PMID:
25564447
2.

Micronucleus frequency among Iraqi thyroid disorder patients.

AlFaisal AH, Al-Ramahi IJ, Abdul-Hassan IA.

Comp Clin Path. 2012 Dec 28;23:683-688. eCollection 2014.

3.

Spirituality, religiosity, and dealing with illness in Arabic and German patients.

Bussing A, Abu-Hassan WM, Matthiessen PF, Ostermann T.

Saudi Med J. 2007 Jun;28(6):933-42.

PMID:
17530114

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