The non-deletion type of alpha thalassaemia/mental retardation: a recognisable dysmorphic syndrome with X linked inheritance.

Author:

Wilkie A O,Pembrey M E,Gibbons R J,Higgs D R,Porteous M E,Burn J,Winter R M

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference6 articles.

1. disease and mental retardation. A new syndrome or a remarkable coincidence?;Weatherall, D.J.; Higgs, D.R.; Bunch, C.;N Engl J Med,1981

2. Clinical features and molecular analysis of the a thalassemia/mental retardation syndromes. I. Cases due to deletions involving chromosome band 16p13.3;Wilkie, A.O.M.; Buckle, V.J.; Harris, P.C.;Am J Hum Genet,1990

3. 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

4. Occurrence of the a thalassaemiamental retardation syndrome (nondeletional type) in an Australian male;Harvey, M.P.; Kearney, A.; Smith, A.; Trent, R.J.;J Med Genet,1990

5. Unknown syndrome. A possible new X linked retardation syndrome: dysmorphic facies, microcephaly, hypotonia, and small genitalia;Porteous, M.E.M.; Bum, J.;J Med Genet,1990

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