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Results 1-10 of 42 (Search time: 0.002 seconds).
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Issue Date
Title
Author(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.
1998
A population-based study of abdominal wall defects in South Australia and Western Australia
Byron-Scott, R.
;
Haan, E.
;
Chan, A.
;
Bower, C.
;
Scott, H.
;
Clark, K.
1998
Transcranial correction of orbital neurofibromatosis
Snyder, B.
;
Hanieh, A.
;
Trott, J.
;
David, D.
1999
Testisin, a new human serine proteinase expressed by premeiotic testicular germ cells and lost in testicular germ cell tumors
Hooper, J.
;
Nicol, D.
;
Dickinson, J.
;
Eyre, H.
;
Scarman, A.
;
Normyle, J.
;
Stuttgen, M.
;
Douglas, M.
;
Loveland, K.
;
Sutherland, G.
;
Antalis, T.
1997
A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome
Muenke, M.
;
Gripp, K.
;
McDonald-McGinn, D.
;
Gaudenz, K.
;
Whitaker, L.
;
Bartlett, S.
;
Markowitz, R.
;
Robin, N.
;
Nwokoro, N.
;
Mulvihill, J.
;
Losken, H.
;
Mulliken, J.
;
Guttmacher, A.
;
Wilroy, R.
;
Clarke, L.
;
Hollway, G.
;
Ades, L.
;
Haan, E.
;
Mulley, J.
;
Cohen, M.
;
et al.
1996
Reduced expression of the interleukin-2-receptor gamma chain on cord blood lymphocytes: relationship to functional immaturity of the neonatal immune response
Zola, H.
;
Fusco, M.
;
Weedon, H.
;
Macardle, P.
;
Ridings, J.
;
Roberton, D.
1999
Homozygotes for FRA16B are normal
Hocking, T.
;
Feichtinger, W.
;
Schmid, M.
;
Haan, E.
;
Baker, E.
;
Sutherland, G.
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.
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.
Discover
Author
9
Haan, E.
8
Roberton, D.
7
Zola, H.
6
Macardle, P.
5
Ridings, J.
4
Ferrante, A.
4
Fusco, M.
4
Weedon, H.
3
Chan, A.
3
Flego, L.
.
next >
Subject
6
Middle Aged
5
Pregnancy
5
Syndrome
4
Australia
4
B-Lymphocytes
4
In Situ Hybridization, Fluorescence
4
Lymphocyte Activation
4
Lymphocytes
4
Molecular Sequence Data
4
Mutation
.
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Date issued
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1999
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1998
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1996
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1995