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Adelaide Research & Scholarship
Adelaide Research & Scholarship
Browsing "Special Research Centre for the Molecular Genetics of Development (CMGD)" by Author Cox, L.
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Issue Date
Title
Author(s)
2000
New mutations in MID1 provide support for loss of function as the cause of X-linked Optiz syndrome
Cox, T.
;
Allen, L.
;
Cox, L.
;
Hopwood, B.
;
Goodwin, B.
;
Haan, E.
;
Suthers, G.
2004
The major splice variant of human 5-aminolevulinate synthase-2 contributes significantly to erythroid heme biosynthesis
Cox, T.
;
Sadlon, T.
;
Schwarz, Q.
;
Matthews, C.
;
Wise, P.
;
Cox, L.
;
Bottomley, S.
;
May, B.