The non-deletion alpha thalassaemia/mental retardation syndrome: further support for X linkage.-Reference-Cited by-同舟云学术

The non-deletion alpha thalassaemia/mental retardation syndrome: further support for X linkage.

Published:1991-11-01 Issue:11 Volume:28 Page:742-745
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Donnai D,Clayton-Smith J,Gibbons R J,Higgs D R

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference5 articles.

1. Clinical features and molecular analysis of the a thalassemia/mental retardation syndromes. II. Cases without detectable abnormality of the a globin complex;Wilkie, A.O.M.; Zeitlin, H.C.; Lindenbaum, R.H.;Am J Hum Genet,1990

2. The chromosomal arrangement of human a-like globin genes: sequence homology and aglobin gene deletions;Lauer, J.; Shen, C.K.J.; Maniatis, T.;Cell,1980

3. The structure of the human zeta-globin gene and a closely linked, nearly identical pseudogene;Proudfoot, N.J.; Gil, A.; Maniatis, T.;Cell,1982

4. Molecular characterisation of a hypervariable region downstream of the human a globin gene cluster;EMBO Jf,1986

5. The non-deletion type of a thalassaemia/mental retardation: a recognisable dysmorphic syndrome with X linked inheritance;Wilkie, A.O.M.; Pembrey, M.E.; Gibbons, R.J.;Jf Med Genet,1991

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