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Items where Author is "Rait, JL"
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Number of items: 3.
Siggs, OM, Souzeau, E, Pasutto, F, Dubowsky, A, Smith, JEH, Taranath, D, Pater, J, Rait, JL, Narita, A, Mauri, L, Del Longo, A, Reis, A, Chappell, A, Kearns, LS, Staffieri, SE, Elder, JE, Ruddle, JB, Hewitt, AW 
ORCID: 0000-0002-5123-5999, Burdon, KP ORCID: 0000-0001-8217-1249, Mackey, DA and Craig, JE 2019
, 'Prevalence of FOXC1 variants in individuals with a suspected diagnosis of primary congenital glaucoma'
, JAMA Ophthalmology, no. Januar
, E1-E8
, doi: https://doi.org/10.1001/jamaophthalmol.2018.5646.
ORCID: 0000-0002-5123-5999, Burdon, KP ORCID: 0000-0001-8217-1249, Mackey, DA and Craig, JE 2019
, 'Prevalence of FOXC1 variants in individuals with a suspected diagnosis of primary congenital glaucoma'
, JAMA Ophthalmology, no. Januar
, E1-E8
, doi: https://doi.org/10.1001/jamaophthalmol.2018.5646.
Souzeau, E, Siggs, OM, Zhou, T, Galanopoulos, A, Hodson, T, Taranath, D, Mills, RA, Landers, J, Pater, J, Smith, JE, Elder, JE, Rait, JL, Giles, P, Phakey, V, Staffieri, SE, Kearns, LS, Dubowsky, A, Mackey, DA, Hewitt, AW ORCID: 0000-0002-5123-5999, Ruddle, JB, Burdon, KP ORCID: 0000-0001-8217-1249 and Craig, JE 2017
, 'Glaucoma spectrum and age-related prevalence of individuals with FOXC1 and PITX2 variants'
, European Journal of Human Genetics, vol. 25, no. 7
, pp. 839-847
, doi: https://doi.org/10.1038/ejhg.2017.59.
ORCID: 0000-0002-5123-5999, Ruddle, JB, Burdon, KP ORCID: 0000-0001-8217-1249 and Craig, JE 2017
, 'Glaucoma spectrum and age-related prevalence of individuals with FOXC1 and PITX2 variants'
, European Journal of Human Genetics, vol. 25, no. 7
, pp. 839-847
, doi: https://doi.org/10.1038/ejhg.2017.59.
Souzeau, E, Siggs, OM, Zhou, T, Galanopoulos, A, Hodson, T, Taranath, D, Mills, RA, Landers, J, Pater, J, Smith, JE, Elder, JE, Rait, JL, Giles, P, Phakey, V, Staffieri, SE, Kearns, LS, Dubowsky, A, Mackey, DA, Hewitt, AW ORCID: 0000-0002-5123-5999, Ruddle, JB, Burdon, KP ORCID: 0000-0001-8217-1249 and Craig, JE 2017
, 'Glaucoma spectrum and age-related prevalence of individuals with FOXC1 and PITX2 variants'
, European Journal of Human Genetics, vol. 25, no. 7
, pp. 839-847
, doi: https://doi.org/10.1038/ejhg.2017.59.
ORCID: 0000-0002-5123-5999, Ruddle, JB, Burdon, KP ORCID: 0000-0001-8217-1249 and Craig, JE 2017
, 'Glaucoma spectrum and age-related prevalence of individuals with FOXC1 and PITX2 variants'
, European Journal of Human Genetics, vol. 25, no. 7
, pp. 839-847
, doi: https://doi.org/10.1038/ejhg.2017.59.