What is the yield of screening echocardiography in pediatric syncope?
Ritter, S, Tani, L Y, Etheridge, S P, Williams, R V, Craig, J E, Minich, L L
Published in Pediatrics (Evanston) (01.05.2000)
Published in Pediatrics (Evanston) (01.05.2000)
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Journal Article
Retinopathy of prematurity: recent advances in our understanding
Wheatley, C M, Dickinson, J L, Mackey, D A, Craig, J E, Sale, M M
Published in Archives of disease in childhood. Fetal and neonatal edition (01.09.2002)
Published in Archives of disease in childhood. Fetal and neonatal edition (01.09.2002)
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Journal Article
Myelodysplastic syndrome with karyotype abnormality is associated with elevated F-cell production
Craig, J E, Sampietro, M, Oscier, D G, Contreras, M, Thein, S
Published in British journal of haematology (01.06.1996)
Published in British journal of haematology (01.06.1996)
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Journal Article
Mutations in LRP5 or FZD4 Underlie the Common Familial Exudative Vitreoretinopathy Locus on Chromosome 11q
Toomes, Carmel, Bottomley, Helen M., Jackson, Richard M., Towns, Katherine V., Scott, Sheila, Mackey, David A., Craig, Jamie E., Jiang, Li, Yang, Zhenglin, Trembath, Richard, Woodruff, Geoffrey, Gregory-Evans, Cheryl Y., Gregory-Evans, Kevin, Parker, Michael J., Black, Graeme C.M., Downey, Louise M., Zhang, Kang, Inglehearn, Chris F.
Published in American journal of human genetics (01.04.2004)
Published in American journal of human genetics (01.04.2004)
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Journal Article
Predictive genetic testing in minors for Myocilin juvenile onset open angle glaucoma
Souzeau, E., Glading, J., Ridge, B., Wechsler, D., Chehade, M., Dubowsky, A., Burdon, K.P., Craig, J.E.
Published in Clinical genetics (01.12.2015)
Published in Clinical genetics (01.12.2015)
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Journal Article
Low Maternal Serum Oestriol at Mid-Trimester May Indicate a Fetal Disorder of Cholesterol Biosynthesis
Craig MBBS, J.E., Savage MSc, V., Cowley FRCPA, D., Clague FRCPA, A., Glass MD, LA
Published in Australian & New Zealand journal of obstetrics & gynaecology (01.05.1999)
Published in Australian & New Zealand journal of obstetrics & gynaecology (01.05.1999)
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Journal Article
Central Corneal Thickness Is Highly Heritable: The Twin Eye Studies
Toh, Tze'Yo, Liew, S. H. Melissa, MacKinnon, Jane R, Hewitt, Alex W, Poulsen, Johan L, Spector, Tim D, Gilbert, Clare E, Craig, Jamie E, Hammond, Christopher J, Mackey, David A
Published in Investigative ophthalmology & visual science (01.10.2005)
Published in Investigative ophthalmology & visual science (01.10.2005)
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Journal Article
Evaluation of optineurin sequence variations in 1,048 patients with open-angle glaucoma
Alward, Wallace L.M, Kwon, Young H, Kawase, Kazuhide, Craig, Jamie E, Hayreh, Sohan S, Johnson, A.Tim, Khanna, Cheryl L, Yamamoto, Tetsuya, Mackey, David A, Roos, Benjamin R, Affatigato, Louisa M, Sheffield, Val C, Stone, Edwin M
Published in American journal of ophthalmology (01.11.2003)
Published in American journal of ophthalmology (01.11.2003)
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Journal Article
Analysis of Myocilin Mutations in 1703 Glaucoma Patients From Five Different Populations
Fingert, John H., Héon, Elise, Liebmann, Jeffrey M., Yamamoto, Tetsuya, Craig, Jamie E., Rait, Julian, Kawase, Kazuhide, Hoh, Sek-Tien, Buys, Yvonne M., Dickinson, Joanne, Hockey, Robin R., Williams-Lyn, Donna, Trope, Graham, Kitazawa, Yoshiaki, Ritch, Robert, Mackey, David A., Alward, Wallace L. M., Sheffield, Val C., Stoned, Edwin M.
Published in Human molecular genetics (01.05.1999)
Published in Human molecular genetics (01.05.1999)
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Journal Article
Aetiology of congenital and paediatric cataract in an Australian population
Wirth, M G, Russell-Eggitt, I M, Craig, J E, Elder, J E, Mackey, D A
Published in British journal of ophthalmology (01.07.2002)
Published in British journal of ophthalmology (01.07.2002)
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Journal Article
A cross-ethnicity investigation of genes previously implicated in primary angle closure glaucoma
Awadalla, Mona S, Burdon, Kathryn P, Thapa, Suman S, Hewitt, Alex W, Craig, Jamie E
Published in Molecular vision (10.08.2012)
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Published in Molecular vision (10.08.2012)
Journal Article
A Spectrum of FOXC1 Mutations Suggests Gene Dosage as a Mechanism for Developmental Defects of the Anterior Chamber of the Eye
Nishimura, Darryl Y., Searby, Charles C., Alward, Wallace L., Walton, David, Craig, Jamie E., Mackey, David A., Kawase, Kazuhide, Kanis, Adam B., Patil, Shivanand R., Stone, Edwin M., Sheffield, Val C.
Published in American journal of human genetics (01.02.2001)
Published in American journal of human genetics (01.02.2001)
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Journal Article
Spectrum and Frequency of FZD4 Mutations in Familial Exudative Vitreoretinopathy
Toomes, Carmel, Bottomley, Helen M, Scott, Sheila, Mackey, David A, Craig, Jamie E, Appukuttan, Binoy, Stout, J. Timothy, Flaxel, Christina J, Zhang, Kang, Black, Graeme C. M, Fryer, Alan, Downey, Louise M, Inglehearn, Chris F
Published in Investigative ophthalmology & visual science (01.07.2004)
Published in Investigative ophthalmology & visual science (01.07.2004)
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Journal Article
Topical prostaglandin f 2α analog induced poliosis
Chen, Celia S., Wells, Jane, Craig, Jamie E.
Published in American journal of ophthalmology (01.05.2004)
Published in American journal of ophthalmology (01.05.2004)
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Journal Article
Spectrum, frequency and penetrance of OPA1 mutations in dominant optic atrophy
Toomes, C, Marchbank, N J, Mackey, D A, Craig, J E, Newbury-Ecob, R A, Bennett, C P, Vize, C J, Desai, S P, Black, G C, Patel, N, Teimory, M, Markham, A F, Inglehearn, C F, Churchill, A J
Published in Human molecular genetics (15.06.2001)
Published in Human molecular genetics (15.06.2001)
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Journal Article
Mutations in a Novel Gene, NHS, Cause the Pleiotropic Effects of Nance-Horan Syndrome, Including Severe Congenital Cataract, Dental Anomalies, and Mental Retardation
Burdon, Kathryn P., McKay, James D., Sale, Michèle M., Russell-Eggitt, Isabelle M., Mackey, David A., Wirth, M. Gabriela, Elder, James E., Nicoll, Alan, Clarke, Michael P., FitzGerald, Liesel M., Stankovich, James M., Shaw, Marie A., Sharma, Shiwani, Gajovic, Srecko, Gruss, Peter, Ross, Shelley, Thomas, Paul, Voss, Anne K., Thomas, Tim, Gécz, Jozef, Craig, Jamie E.
Published in American journal of human genetics (01.11.2003)
Published in American journal of human genetics (01.11.2003)
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Journal Article
Prevalence of CYP1B1 mutations in Australian patients with primary congenital glaucoma
Dimasi, DP, Hewitt, AW, Straga, T, Pater, J, MacKinnon, JR, Elder, JE, Casey, T, Mackey, DA, Craig, JE
Published in Clinical genetics (01.09.2007)
Published in Clinical genetics (01.09.2007)
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