Cooperative sequence modules determine replication initiation sites at the human -globin locus

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Oxford University Press

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Developmentally distinct effects on human  -, γ - and  -globin levels caused by the absence or altered position of the human β -globin gene in YAC transgenic mice

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A Novel Mechanism Generating Short Deletion/Insertions Following Slippage is Suggested by a Mutation in the Human α 2 -Globin Gene

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A familial GLI2 deletion (2q14.2) not associated with the holoprosencephaly syndrome phenotype

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Two further patients with the 1q24 deletion syndrome expand the phenotype: A possible role for the miR199–214 cluster in the skeletal features of the condition

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