Occurrence of the alpha thalassaemia-mental retardation syndrome (non-deletional type) in an Australian male.

Author:

Harvey M P,Kearney A,Smith A,Trent R J

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference20 articles.

1. Human (t-globin maps to pter-pl3.3 in chromosome 16 distal to PGP;Breuning, M.H.; Madan, K.; Verjaal, M.; Wijnen, J.T.; Meera Khan, P.; Pearson, P.L.;Hum Genet,1987

2. Higgs DR, Vickers MA, Wilkie AOM, Pretorius IM, Jarman AP, Weatherall DJ. A review of the molecular genetics of the human alpha-globin gene cluster. Blood 1989;73: 1081-104.

3. disease and mental retardation-a new syndrome or a remarkable coincidence?;Weatherall, J.; Higgs, D.R.; Bunch, C.;N Engl 7 Med,1981

4. Hemoglobin-H disease in association with multiple congenital abnormalities;Borochowitz, D.; Levin, S.E.; Krawitz, S.; Stevens, K.; Metz, J.;Clin Pediatr,1970

5. The hemoglobin H disease mental retardation syndrome: molecular studies on the South African case;Bowcock, A.M.; van Tonder, S.; Jenkins, T.,1984

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