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Issue Date
Title
Author(s)
1998
Transcranial correction of orbital neurofibromatosis
Snyder, B.
;
Hanieh, A.
;
Trott, J.
;
David, D.
1998
Evaluation of the lysosome-associated membrane protein LAMP-2 as a marker for lysosomal storage disorders
Hua, C.
;
Hopwood, J.
;
Carlsson, S.
;
Harris, R.
;
Meikle, P.
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
Autosomal dominant Klippel-Feil anomaly with cleft palate
Thompson, E.
;
Haan, E.
;
Sheffield, 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.
Discover
Author
2
Hopwood, J.
1
Aldis, J.
1
Berkovic, S.
1
Blanch, L.
1
Carlsson, S.
1
Colman, P.
1
Couper, J.
1
David, D.
1
Ferrante, A.
1
Guo, X.H.
.
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Subject
1
Bone Transplantation
1
Chromosomes, Human, Pair 2
1
Cleft Palate
1
Craniotomy
1
Diabetes Mellitus, Type 1
1
Disease Progression
1
Electroencephalography
1
Electrophoresis, Polyacrylamide Gel
1
Enophthalmos
1
Enzyme-Linked Immunosorbent Assay
.
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