(Q33597042)

28 July 2017

Localisation of the MRX3 gene for non-specific X linked mental retardation (English)

1 reference

28 July 2017

Gedeon A

1

1 reference

28 July 2017

Kerr B

series ordinal

2

1 reference

28 July 2017

Mulley J

series ordinal

3

1 reference

28 July 2017

Turner G

series ordinal

4

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 June 1991

1 reference

Journal of Medical Genetics

28 July 2017

1 reference

28 July 2017

28

1 reference

28 July 2017

372-377

1 reference

28 July 2017

6

1 reference

X-linked mental retardation.

28 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016900

X-linked mental retardation and verbal disability.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016900

Multilocus linkage analysis in humans: detection of linkage and estimation of recombination

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016900

Localization of the gene for a syndrome of X-linked skeletal dysplasia and mental retardation to Xq27-qter.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016900

Linkage studies of X-linked recessive spastic paraplegia using DNA probes.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016900

A non-syndromal form of X-linked mental retardation (XLMR) is linked to DXS14.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016900

Linkage analysis suggests at least two loci for X-linked non-specific mental retardation.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016900

Is there a fragile(X) negative Martin-Bell syndrome?

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016900

MASA syndrome: further clinical delineation and chromosomal localisation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016900

Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016900

Report of the committee on clinical disorders and chromosomal deletion syndromes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016900

Report of the committee on cytogenetic markers

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016900

Physical mapping of new DNA probes near the fragile X mutation (FRAXA) by using a panel of cell lines

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016900

Genetic counseling in rare syndromes: a resampling method for determining an approximate confidence interval for gene location with linkage data from a single pedigree

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016900

MASA syndrome: new clinical features and linkage analysis using DNA probes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016900

Non-specific X linked mental retardation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016900

A computer program for linkage analysis of general human pedigrees

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016900

Linkage and genetic counselling for the fragile X using DNA probes 52A, F9, DX13, and ST14

21 June 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/1870093

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JMG.28.6.372

1 reference

28 July 2017

1 reference

28 July 2017

1 reference