Skip to main content

. 1991 Oct;28(10):724. doi: 10.1136/jmg.28.10.724

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

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

PMCID: PMC1017065 PMID: 1941971

724

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

Bloch M., Hayden M. R. Opinion: predictive testing for Huntington disease in childhood: challenges and implications. Am J Hum Genet. 1990 Jan;46(1):1–4. [PMC free article] [PubMed] [Google Scholar]
Bloch M., Hayden M. R. Opinion: predictive testing for Huntington disease in childhood: challenges and implications. Am J Hum Genet. 1990 Jan;46(1):1–4. [PMC free article] [PubMed] [Google Scholar]
Harvey M. P., Kearney A., Smith A., Trent R. J. Occurrence of the alpha thalassaemia-mental retardation syndrome (non-deletional type) in an Australian male. J Med Genet. 1990 Sep;27(9):577–581. doi: 10.1136/jmg.27.9.577. [DOI] [PMC free article] [PubMed] [Google Scholar]
Porteous M. E., Burn J. Unknown syndrome. A possible new X linked retardation syndrome: dysmorphic facies, microcephaly, hypotonia, and small genitalia. J Med Genet. 1990 May;27(5):339–340. doi: 10.1136/jmg.27.5.339. [DOI] [PMC free article] [PubMed] [Google Scholar]
Weatherall D. J., Higgs D. R., Bunch C., Old J. M., Hunt D. M., Pressley L., Clegg J. B., Bethlenfalvay N. C., Sjolin S., Koler R. D. Hemoglobin H disease and mental retardation: a new syndrome or a remarkable coincidence? N Engl J Med. 1981 Sep 10;305(11):607–612. doi: 10.1056/NEJM198109103051103. [DOI] [PubMed] [Google Scholar]

ACTIONS

RESOURCES