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Eye (London, England)|August 14, 2010
Cone-rod dystrophy and amelogenesis imperfecta (Jalili syndrome): phenotypes and environsI K JaliliJournal of Medical Genetics|August 1, 1989
Cone-rod congenital amaurosis associated with congenital hypertrichosis: an autosomal recessive conditionI K JaliliEye (London, England)|July 31, 1998
Congenital-onset central chorioretinal dystrophy associated with high myopiaM Iqbal, I K JaliliJournal of Medical Genetics|November 1, 1988
A progressive cone-rod dystrophy and amelogenesis imperfecta: a new syndromeI K Jalili, N J SmithJournal of the Mechanical Behavior of Biomedical Materials|February 21, 2019
In situ probing of switchable nanomechanical properties of responsive high-density polymer brushes on poly(dimethylsiloxane): An AFM nanoindentation approachK Jalili, F Abbasi, L BehboodpourJournal of Biomaterials Science. Polymer Edition|November 30, 2020
Multi-layer PDMS films having antifouling property for biomedical applicationsM Mousavi, H Ghaleh, K Jalili, et al.Journal of the Mechanical Behavior of Biomedical Materials|July 25, 2009
Relationships between the morphology, swelling and mechanical properties of poly(dimethyl siloxane)/poly(acrylic acid) interpenetrating networksK Jalili, F Abbasi, S S Oskoee, et al.Human Genetics|July 1, 1991
Increased band sharing in DNA fingerprints of an inbred human populationR J Bellamy, C F Inglehearn, I K Jalili, et al.European Journal of Human Genetics : EJHG|December 4, 2002
Identification of a locus on chromosome 2q11 at which recessive amelogenesis imperfecta and cone-rod dystrophy cosegregateLouise M Downey, T Jeffrey Keen, Ismail K Jalili, et al.American Journal of Human Genetics|February 10, 2009
Mutations in CNNM4 cause Jalili syndrome, consisting of autosomal-recessive cone-rod dystrophy and amelogenesis imperfectaDavid A Parry, Alan J Mighell, Walid El-Sayed, et al.Pageof 1