(Q41671994)

6 October 2017

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

1 reference

Andrew Oliver Mungo Wilkie

6 October 2017

1

1 reference

6 October 2017

Pembrey ME

2

1 reference

6 October 2017

Gibbons RJ

3

1 reference

6 October 2017

Higgs DR

4

1 reference

6 October 2017

Porteous ME

5

1 reference

6 October 2017

Burn J

6

1 reference

6 October 2017

Winter RM

7

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6 October 2017

language of work or name

English

0 references

publication date

1 October 1991

1 reference

Journal of Medical Genetics

6 October 2017

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6 October 2017

28

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6 October 2017

10

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6 October 2017

724

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Hemoglobin H disease and mental retardation: a new syndrome or a remarkable coincidence?

6 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017065

Unknown syndrome. A possible new X linked retardation syndrome: dysmorphic facies, microcephaly, hypotonia, and small genitalia

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017065

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

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017065

Opinion: predictive testing for Huntington disease in childhood: challenges and implications

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017065

6 June 2018

Identifiers

DOI

10.1136/JMG.28.10.724

1 reference

6 October 2017

1 reference

6 October 2017

PubMed publication ID

1941971

1 reference