(Q33597729)

28 July 2017

1 reference

title

A newly defined X linked mental retardation syndrome associated with alpha thalassaemia (English)

1 reference

Andrew Oliver Mungo Wilkie

28 July 2017

author

series ordinal

2

1 reference

28 July 2017

Gibbons RJ

1

1 reference

28 July 2017

Weatherall DJ

series ordinal

3

1 reference

28 July 2017

Higgs DR

series ordinal

4

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 November 1991

1 reference

Journal of Medical Genetics

28 July 2017

published in

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28 July 2017

volume

28

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28 July 2017

issue

11

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28 July 2017

page(s)

729-733

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

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017105

A review of the molecular genetics of the human alpha-globin gene cluster

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017105

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017105

Clinical features and molecular analysis of the alpha thalassemia/mental retardation syndromes. I. Cases due to deletions involving chromosome band 16p13.3.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017105

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017105

Globin gene regulation and switching: circa 1990.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017105

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017105

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017105

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017105

X linked alpha thalassaemia/mental retardation: spectrum of clinical features in three related males

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017105

Alpha thalassaemia/mental retardation syndrome (non-deletional type): report of a family supporting X linked inheritance

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017105

21 June 2018

Identifiers

DOI

10.1136/JMG.28.11.729

1 reference

28 July 2017

1 reference

28 July 2017

1 reference