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Issue Date
Title
Author(s)
1997
Mapping of the gene for vascular endothelial growth factor-D in mouse and man to the X chromosome
Jenkins, N.
;
Woollatt, E.
;
Crawford, J.
;
Gilbert, D.
;
Baldwin, M.
;
Sutherland, G.
;
Copeland, N.
;
Achen, M.
1999
A template for defining a causal relation between acute intrapartum events and cerebral palsy: international consensus statement
MacLennan, A.
1995
Exposure to environmental lead and visual motor integration at 7 years: The Port Pirie Cohort Study
Baghurst, P.
;
McMichael, A.
;
Tong, S.
;
Wigg, N.
;
Vimpani, G.
;
Robertson, E.
1996
Children with hyperimmunoglobulinemia D and periodic fever syndrome
Grose, C.
;
Schnetzer, J.
;
Ferrante, A.
;
Vladutiu, A.
1997
Genomic structure and complete nucleotide sequence of the Batten Disease Gene, CLN3
Mitchison, H.
;
Munroe, P.
;
O'Rawe, A.
;
Taschner, P.
;
De Vos, N.
;
Kremmidiotis, G.
;
Lensink, I.
;
Munk, A.
;
D'Arigo, K.
;
Anderson, J.
;
Lerner, T.
;
Moyzis, R.
;
Callen, D.
;
Breuning, M.
;
Doggett, N.
;
Gardiner, R.
;
Mole, S.
1995
Mechanisms of small ring formation suggested by the molecular characterization of 2 small accessory ring chromosomes derived from chromosome 4
Fang, Y.
;
Eyre, H.
;
Bohlander, S.
;
Estop, A.
;
McPherson, E.
;
Trager, T.
;
Riess, O.
;
Callen, D.
1995
Activation of the neutrophil bactericidal activity for non-typable Haemophilus influenzae by tumor necrosis factor and lymphotoxin
Tan, A.M.
;
Ferrante, A.
;
Goh, D.
;
Roberton, D.
;
Cripps, A.
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.
1998
Coexistence of Gaucher-Disease Type 1 and Joubert-Syndrome
Van Royen-Kerkhof, A.
;
Pollthe, B.
;
Kleijer, W.
;
van Diggelen, O.
;
Aerts, J.
;
Hopwood, J.
;
Beemer, F.
1996
Identification, expression, and biochemical characterization of N-acetylgalactosamine-4-sulfatase mutations and relationship with clinical phenotype in MPS-VI patients
Litjens, T.
;
Brooks, D.
;
Peters, C.
;
Gibson, G.
;
Hopwood, J.
Discover
Author
69
Sutherland, G.
39
Hopwood, J.
28
Haan, E.
27
Baker, E.
26
Ferrante, A.
20
Norman, R.
18
Eyre, H.
16
Poulos, A.
16
Roberton, D.
14
Robinson, J.
.
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Subject
46
Infant, Newborn
45
Adolescent
44
Child, Preschool
43
Amino Acid Sequence
36
In Situ Hybridization, Fluorescence
31
Infant
29
Cloning, Molecular
28
DNA, Complementary
26
Mice
26
Middle Aged
.
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