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Vanin, E.
( E. Vanin)
deletion sequence breakpoint probe fragment globin cluster result chromosome figure region family hybridization rearrangement event clone point hpfh 1 order nature p-globin deletion event &3-thal research ill-barn hi fragment restriction amount hpfh 2 cosmid study phage orkin replication eco ri alui family sequences acids research dna sequences sph 2.5 probe alu sequence exchange 2.5 deletion joints mechanism dna loops relationship genomic dna p-globin gene flavell breakage reunion event chromosome 11. nucleotide thalassaemia van der ploeg kpni family sequence number hpfh 1 deletion length p-globin gene cluster hpfh 2 homozygote restriction enzyme sites fritsch y &3-thal 1 alu family sequence sph 2.5 nonhomologou figure 3 persistence nucleotide sequences thalassemia distance cosmid clones anchorage hybridization studies genomic attachment points anchorage points enzyme hybridize hemoglobin
3 Most Recent Publications
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γδβ-thalassaemias 1 and 2 are the result of a 100 kpb deletion in the human β-globin cluster.
(Article)
Taramelli, R. Kioussis, D. Vanin, E. Bartram, K. Groffen, J. Hurst, J. Grosveld, F.G. |
1986-01-01
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β-globin gene inactivation by DNA translocation in γ β-thalassaemia.
(Miscellaneous)
Kioussis, D. Vanin, E. Lange, T. de Flavell, R.A. Grosveld, F.G. |
1983-01-01
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Unexpected relationships between four large deletions in the human β-globin gene cluster.
(Article)
Vanin, E. Henthorn, P. Kioussis, D. Grosveld, F.G. Smithies, O. |
1983-01-01
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