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Issue Date
Title
Author(s)
1998
A novel mutation in exon b (R259C) of the MTM1 gene is associated with a mild myotubular myopathy.
Donnelly, A.
;
Haan, E.
;
Manson, J.
;
Mulley, J.
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
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.
1998
The impact of rubella immunisation on the incidence of rubella, congenital rubella syndrome and rubella-related terminations of pregnancy in South Australia
Cheffins, T.
;
Chan, A.
;
Keane, R.
;
Haan, E.
;
Hall, R.
Discover
Author
1
Ades, L.
1
Chan, A.
1
Cheffins, T.
1
Cleary, E.
1
Donnelly, A.
1
Ellis, S.
1
Gibson, M.
1
Hall, R.
1
Keane, R.
1
Manson, J.
.
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Subject
5
Humans
3
Child
3
Female
2
Adult
2
Exons
2
Mutation
2
Radiography
1
Abnormalities, Multiple
1
Abortion, Induced
1
Abortion, Spontaneous
.
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