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Results 1-10 of 10 (Search time: 0.004 seconds).
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Issue Date
Title
Author(s)
1998
Transcranial correction of orbital neurofibromatosis
Snyder, B.
;
Hanieh, A.
;
Trott, J.
;
David, D.
1998
Asthma and other atopic diseases in Australian children. Australian arm of the International Study of Asthma and Allergy in Childhood
Robertson, C.
;
Dalton, M.
;
Peat, J.
;
Haby, M.
;
Bauman, A.
;
Kennedy, J.
;
Landau, L.
1998
Haemolytic-uraemic syndrome outbreak caused by Escherichia coli O111:H-: clinical outcomes
Henning, P.
;
Tham, E.
;
Martin, A.
;
Beare, T.
;
Jureidini, K.
1998
Identification of a common mutation (R245h) in Sanfilippo A patients from the Netherlands
Weber, B.
;
Vandekamp, J.
;
Kleijer, W.
;
Guo, X.H.
;
Blanch, L.
;
van Diggelen, O.
;
Wevers, R.
;
Poorthuis, B.
;
Hopwood, J.
1998
Familial partial epilepsy with variable foci: A new partial epilepsy syndrome with suggestion of linkage to chromosome 2
Scheffer, I.
;
Phillips, H.
;
O'Brien, C.
;
Saling, M.
;
Wrennall, J.
;
Wallace, R.
;
Mulley, J.
;
Berkovic, S.
1998
Two unusual cases of megacolons
Chacko, J.
;
Sparnon, A.
;
Little, K.
1998
Autosomal dominant Klippel-Feil anomaly with cleft palate
Thompson, E.
;
Haan, E.
;
Sheffield, L.
1998
SHORT syndrome: distinctive radiographic features
Haan, E.
;
Morris, L.
1998
IgG subclass antibodies to glutamic acid decarboxylase and risk for progression to clinical insulin-dependent diabetes
Couper, J.
;
Harrison, L.
;
Aldis, J.
;
Colman, P.
;
Honeyman, M.
;
Ferrante, A.
1998
Preferential pre-mRNA utilisation of an upstream cryptic 5' splice site created by a single base deletion mutation in exon 37 of the FBN-1 gene
Gibson, M.
;
Ellis, S.
;
Ades, L.
;
Haan, E.
;
Cleary, E.
Discover
Author
3
Haan, E.
1
Ades, L.
1
Aldis, J.
1
Bauman, A.
1
Beare, T.
1
Berkovic, S.
1
Blanch, L.
1
Chacko, J.
1
Cleary, E.
1
Colman, P.
.
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2
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2
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2
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