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Issue Date
Title
Author(s)
1996
Long-term in vitro correction of alpha-L-iduronidase deficiency (Hurler syndrome) in human bone marrow
Fairbairn, L.
;
Lashford, L.
;
Spooncer, E.
;
McDermott, R.
;
Lebens, G.
;
Arrand, J.
;
Arrand, J.
;
Bellantuono, I.
;
Holt, R.
;
Hatton, C.
;
Cooper, A.
;
Besley, G.
;
Wraith, J.
;
Anson, D.
;
Hopwood, J.
;
Dexter, T.
2008
X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment
Dibbens, L.
;
Tarpey, P.
;
Hynes, K.
;
Bayly, M.
;
Scheffer, I.
;
Smith, R.
;
Bomar, J.
;
Sutton, E.
;
Vandeleur, L.
;
Shoubridge, C.
;
Edkins, S.
;
Turner, S.
;
Stevens, C.
;
O'Meara, S.
;
Tofts, C.
;
Barthorpe, S.
;
Buck, G.
;
Cole, J.
;
Halliday, K.
;
Jones, D.
;
et al.
2000
FMR3 is a novel gene associated with FRAXE CpG island and transcriptionally silent in FRAXE full mutations
Gecz, J.
1997
Most germ-line mutations in the nevoid basal cell carcinoma syndrome lead to a premature termination of the PATCHED protein, and no genotype-phenotype correlations are evident
Wicking, C.
;
Shanley, S.
;
Smyth, I.
;
Gillies, S.
;
Negus, K.
;
Graham, S.
;
Suthers, G.
;
Haites, N.
;
Edwards, M.
;
Wainwright, B.
;
Chenevix Trench, G.
2007
Mutations in ZDHHC9, which encodes a palmitoyltransferase of NRAS and HRAS, cause X-linked mental retardation associated with a marfanoid habitus
Raymond, F.
;
Tarpey, P.
;
Edkins, S.
;
Tofts, C.
;
O'Meara, S.
;
Teague, J.
;
Butler, A.
;
Stevens, C.
;
Barthorpe, S.
;
Buck, G.
;
Cole, J.
;
Dicks, E.
;
Gray, K.
;
Harrison, R.
;
Hills, K.
;
Hinton, J.
;
Jones, D.
;
Menzies, A.
;
Perry, J.
;
Raine, K.
;
et al.
2022
The phenotypic spectrum of ADAMTSL4-associated ectopia lentis: Additional cases, complications, and review of literature
Knight, L.S.W.
;
Mullany, S.
;
Taranath, D.A.
;
Ruddle, J.B.
;
Barnett, C.P.
;
Sallevelt, S.C.E.H.
;
Berry, E.C.
;
Marshall, H.N.
;
Hollitt, G.L.
;
Souzeau, E.
;
Craig, J.E.
;
Siggs, O.M.
1998
X-linked adrenoleukodystrophy: the Australasian experience
Kirk, E.
;
Fletcher, J.
;
Sharp, P.
;
Carey, B.
;
Poulos, A.
1997
Unbalanced t(4;11)(q32-q23) in a 34-year-old man with manifestations of distal monosomy 11q and trisomy 4q syndromes
Byatt, S.
;
Baker, E.
;
Richards, R.
;
Roberts, C.
;
Smith, A.
2003
Induction of tolerance to a recombinant human enzyme, acid alpha-glucosidase, in enzyme deficient knockout mice
Raben, N.
;
Nagaraju, K.
;
Lee, A.
;
Lu, N.
;
Rivera, Y.
;
Jatkar, T.
;
Hopwood, J.
;
Plotz, P.
2020
Evaluation of DNA methylation episignatures for diagnosis and phenotype correlations in 42 mendelian neurodevelopmental disorders
Aref-Eshghi, E.
;
Kerkhof, J.
;
Pedro, V.P.
;
Barat-Houari, M.
;
Ruiz-Pallares, N.
;
Andrau, J.C.
;
Lacombe, D.
;
Van-Gils, J.
;
Fergelot, P.
;
Dubourg, C.
;
Cormier-Daire, V.
;
Rondeau, S.
;
Lecoquierre, F.
;
Saugier-Veber, P.
;
Nicolas, G.
;
Lesca, G.
;
Chatron, N.
;
Sanlaville, D.
;
Vitobello, A.
;
Faivre, L.
;
et al.
Discover
Author
19
Gecz, J.
19
Hopwood, J.
10
et al.
7
Haan, E.
6
Scheffer, I.
5
Brooks, D.
5
Mulley, J.
5
Weber, B.
5
Yogalingam, G.
4
Berkovic, S.
.
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Male
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19
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Date issued
2
2020 - 2022
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2010 - 2019
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2000 - 2009
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1995 - 1999