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Search Results - Dahl, H.H.M
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The construction of cosmid libraries which can be used to transform eukaryotic cells
by
Grosveld, F.G.
,
Lund, T.
,
Murray, E.J.
,
Mellor, A.L
,
Dahl, H.H.M.
,
Flavell, R.A.
Published in
Nucleic acids research
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Pyruvate dehydrogenase deficiency caused by a 5 base pair duplication in the E1α subunit
by
Hansen, L.L.
,
Brown, G.K.
,
Brown, R.M.
,
Dahl, H.H.M.
Published in
Human molecular genetics
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Mitochondrial myopathy with tRNALeu(UUR) mutation and complex I deficiency responsive to riboflavin
by
Ogle, R.F. (Royal Alexandra Hospital for Children, Westmead, New South Wales, Australia.)
,
Christodoulou, J
,
Fagan, E
,
Blok, R.B
,
Kirby, D.M
,
Seller, K.L
,
Dahl, H.H.M
,
Thorburn, D.R
Published in
The Journal of pediatrics
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effect of streptozotocin-induced diabetes on phenylalanine hydroxylase expression in rat liver
by
Taylor, D.S
,
Dahl, H.H.M
,
Mercer, J.F.B
,
Green, A.K
,
Fisher, M.J
Published in
Biochemical journal
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Structure and expression of a cloned β°thalassaemic globin gene
by
Moschonas, N.
,
de Boer, E.
,
Grosveld, F.G.
,
Dahl, H.H.M.
,
Wright, S.
,
Shewmaker, C.K.
,
Flavell, R.A.
Published in
Nucleic acids research
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Application of DNA-DNA hybridization of dual labeled probes to the detection of trisomy 21, monosomy 21, and sex determination
by
DAHL, H.-H. M
,
CHOO, K. H
,
DANKS, D. M
Published in
American journal of human genetics
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mtDNA Deletion in a Patient with Symptoms of Mitochondrial Cytopathy but without Ragged Red Fibers
by
Blok, R.B.
,
Thorburn, D.R.
,
Danks, D.M.
,
Dahl, H.H.M.
Published in
Biochemical and molecular medicine
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