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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.
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.
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.
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.
2007
The mental health and wellbeing of children and adolescents in home-based foster care
Sawyer, M.
;
Carbone, J.
;
Searle, A.
;
Robinson, P.
2003
MJA Practice Essentials - 2: Recent advances in therapy of diabetes - Endocrinology
Couper, J.
;
Prins, J.
2003
Two further cases of Ohdo syndrome delineate the phenotypic variability of the condition
White, S.
;
Ades, L.
;
Amor, D.
;
Liebelt, J.
;
Bankier, A.
;
Baker, E.
;
Wilson, M.
;
Savarirayan, R.
2008
Effect of long-chain polyunsaturated fatty acid supplementation of preterm infants on disease risk and neurodevelopment: a systematic review of randomized controlled trials
Smithers, L.
;
Gibson, R.
;
McPhee, A.
;
Makrides, M.
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.
Discover
Author
52
Gecz, J.
43
et al.
41
Haan, E.
40
Sutherland, G.
33
Davidson, G.
30
Hopwood, J.
22
Anderson, P.J.
22
Makrides, M.
21
Couper, J.
21
Omari, T.
.
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Subject
78
Mutation
71
Pedigree
64
Middle Aged
61
Australia
54
Molecular Sequence Data
44
Mice
41
Intellectual Disability
40
Base Sequence
37
Chromosome Mapping
37
Follow-Up Studies
.
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