Browsing by Author Prokudin, Ivan

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Issue DateTitleAuthor(s)Citation
2014Detection of Chromosomal Breakpoints in Patients with Developmental Delay and Speech DisordersJamieson, Robyn; Prokudin, Ivan; Yousoof, Saira; Aksoy, Irene; Chen, Pauline J; Chew, Elaine G Y; et al, .; Hillmer, Axel M; Lee, Charlie W H; Seng, Chan Chee; Teo, Audrey S M; Utami, Kagistia H; Zhang, Zhenshui; Children's Hospital Westmead: Paediatrics & Child Health; Central Clinical School: Ophthalmology & Eye Health; Children's Hospital Westmead: Paediatrics & Child HealthDetection of Chromosomal Breakpoints in Patients with Developmental Delay and Speech Disorders, PLoS One, vol.9, 3, 2014,pp 1-10
2015Mutations in SIPA1L3 cause eye defects through disruption of cell polarity and cytoskeleton organizationBecker, Thomas; Cheng, Anson; Greenlees, Rebecca; Grigg, John; Jamieson, Robyn; Loebel, David; Ma, Alan; Mihelec, Marija; Nash, Benjamin; Prokudin, Ivan; Rinkwitz, Silke; Speidel, Daniel; Tam, Patrick; Yousoof, Saira Bahnu Mohamed; Black, Graeme C M; Clayton-Smith, Jill; Gillespie, Rachel; Lloyd, I. Christopher; Perveen, Rahat; Semina, Elena; Wu, Selwin K; Yap, Alpha; School of Medical Sciences: Brain and Mind Centre; Central Clinical School: Save Sight & Eye Health Inst.; Biological Sciences; Central Clinical School: Clinical Ophthal & Eye Health; Childrens Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Childrens Medical Research Ins; School of Medical Sciences: Pathology; Central Clinical School: Save Sight & Eye Health Inst.; Children's Hospital Westmead: Childrens Medical Research Ins; Central Clinical School: Ophthalmology & Eye Health; School of Medical Sciences: Brain and Mind Centre; Children's Hospital Westmead: Childrens Medical Research Ins; Children's Hospital Westmead: Childrens Medical Research Ins; SAHCS: Clinical Ophthalmology and Eye HealthMutations in SIPA1L3 cause eye defects through disruption of cell polarity and cytoskeleton organization, Human Molecular Genetics, vol.24, 20, 2015,pp 5789-5804
2016Sporadic and Familial Congenital Cataracts: Mutational Spectrum and new Diagnoses using Next-Generation SequencingBennetts, Bruce; Billson, Frank; Cheng, Anson; Christodoulou, John; Flaherty, Maree; Fraser, Clare; Grigg, John; Jamieson, Robyn; Ma, Alan; Martin, Frank; Prokudin, Ivan; Farnsworth, Elizabeth; Ho, Gladys; Holman, katherine; Mowat, David; Smith, James; Childrens Hospital Westmead: Paediatrics & Child Health; Central Clinical School: Clinical Ophthal & Eye Health; Central Clinical School: Save Sight & Eye Health Inst.; Childrens Hospital Westmead: Paediatrics & Child Health; Central Clinical School: Clinical Ophthal & Eye Health; Central Clinical School: Save Sight & Eye Health Inst.; Central Clinical School: Clinical Ophthal & Eye Health; Childrens Medical Research Institute (CMRI); Children's Hospital Westmead: Genetic Medicine; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Medical Research Institute (CMRI)Sporadic and Familial Congenital Cataracts: Mutational Spectrum and new Diagnoses using Next-Generation Sequencing, Human Mutation, vol.37, 4, 2016,pp 371-384