Allan-Herndon-Dudley syndrome and the monocarboxylate transporter 8 (MCT8) gene (Q24533641)

4 July 2017

Allan-Herndon-Dudley syndrome and the monocarboxylate transporter 8 (MCT8) gene (English)

1 reference

Allan-Herndon-Dudley syndrome

4 July 2017

1 reference

Charles E Schwartz

1

1 reference

4 July 2017

Melanie M May

2

1 reference

4 July 2017

Nancy J Carpenter

3

1 reference

4 July 2017

R Curtis Rogers

4

1 reference

4 July 2017

Judith Martin

5

1 reference

4 July 2017

Martin G Bialer

6

1 reference

4 July 2017

Jewell Ward

7

1 reference

4 July 2017

Javier Sanabria

8

1 reference

4 July 2017

Silvana Marsa

9

1 reference

4 July 2017

James A Lewis

10

1 reference

4 July 2017

Roberto Echeverri

11

1 reference

4 July 2017

Herbert A Lubs

12

1 reference

4 July 2017

Kytja Voeller

13

1 reference

4 July 2017

Richard J Simensen

14

1 reference

4 July 2017

Roger E Stevenson

15

1 reference

4 July 2017

language of work or name

English

0 references

publication date

11 May 2005

1 reference

American Journal of Human Genetics

4 July 2017

1 reference

4 July 2017

77

1 reference

4 July 2017

41-53

1 reference

4 July 2017

1

1 reference

A PEDIGREE OF MENTAL DEFECT SHOWING SEX-LINKAGE.

4 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226193

A novel syndrome combining thyroid and neurological abnormalities is associated with mutations in a monocarboxylate transporter gene

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226193

24 March 2017

A marker X chromosome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226193

Association between mutations in a thyroid hormone transporter and severe X-linked psychomotor retardation

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226193

Clinical and molecular contributions to the understanding of X-linked mental retardation

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226193

Allan-Herndon syndrome. II. Linkage to DNA markers in Xq21

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226193

Allan-Herndon syndrome. I. Clinical studies

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226193

Allan-Herndon-Dudley syndrome: clinical and linkage studies on a second family.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226193

X-linked spastic paraplegia and Pelizaeus-Merzbacher disease are allelic disorders at the proteolipid protein locus

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226193

Fine mapping and clinical reevaluation of a Brazilian pedigree with a severe form of X-linked mental retardation associated with other neurological dysfunction.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226193

Hereditary mental defect showing the pattern of sex influence.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226193

MASA syndrome is due to mutations in the neural cell adhesion gene L1CAM.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226193

Thyroid hormone transporters

29 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15889350

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1086/431313

1 reference

OpenCitations bibliographic resource ID

4 July 2017

2003286

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

4 July 2017

1 reference