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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.
2002
Isolation and characterisation of the chick orthologue of the Opitz syndrome gene, Mid1, supports a conserved role in vertebrate development
Richman, J.
;
Fu, K.
;
Cox, L.
;
Sibbons, J.
;
Cox, T.
2003
Expression of three spalt (sal) gene homologues in zebrafish embryos
Camp-Dotlic, E.
;
Hope, R.
;
Kortschak, R.
;
Cox, T.
;
Lardelli, M.
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.
2004
Analysis of intracranial volume in Apert Syndrome genotypes
Anderson, P.
;
Netherway, D.
;
Abbott, A.
;
Cox, T.
;
Roscioli, T.
;
David, D.
2000
Gene structure and expression study of the SEDL gene for Spondyloepiphyseal Dysplasia Tarda
Gecz, J.
;
Hillman, M.
;
Gedeon, A.
;
Cox, T.
;
Baker, E.
;
Mulley, J.
2002
Complementation of a yeast CYC3 deficiency identifies an X-linked mammalian activator of apocytochrome c
Schwarz, Q.
;
Cox, T.
Discover
Author
3
Cox, L.
2
Schwarz, Q.
1
Abbott, A.
1
Allen, L.
1
Anderson, P.
1
Baker, E.
1
Bottomley, S.
1
Camp-Dotlic, E.
1
David, D.
1
Fu, K.
.
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Subject
4
Humans
3
Female
3
Male
2
Exons
2
Genetic Linkage
2
Transcription Factors
2
X Chromosome
1
3T3 Cells
1
5-Aminolevulinate synthase
1
Abnormalities, Multiple
.
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Date issued
2
2004
1
2003
2
2002
2
2000