(Q41783824)

9 October 2017

Molecular evidence that fragile X syndrome occurs in the South African black population (English)

1 reference

9 October 2017

0 references

1 reference

Goldman A

1

1 reference

9 October 2017

Jenkins T

series ordinal

2

1 reference

9 October 2017

Krause A

series ordinal

3

1 reference

9 October 2017

language of work or name

English

0 references

publication date

1 October 1998

1 reference

Journal of Medical Genetics

9 October 2017

1 reference

9 October 2017

35

1 reference

9 October 2017

10

1 reference

9 October 2017

878

1 reference

Prevalence of carriers of premutation-size alleles of the FMRI gene--and implications for the population genetics of the fragile X syndrome.

9 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051470

The Martin-Bell syndrome in South Africa

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051470

Fragile X syndrome: incidence, clinical and cytogenetic findings in the black and white populations of South Carolina

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051470

Frequency of Fra X syndrome among institutionalized mentally retarded males in Poland.

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051470

A marker X chromosome associated with nonspecific male mental retardation. The first South African cases

18 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051470

Comparison between the cytogenetic test for fragile X and the molecular analysis of the FMR-1 gene in Japanese mentally retarded individuals

18 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9783718

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Fragile X syndrome occurs in the South African black population

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9783718

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

DNA diagnosis of the fragile X syndrome in a series of 236 mentally retarded subjects and evidence for a reversal of mutation in the FMR-1 gene

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9783718

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JMG.35.10.878

1 reference

9 October 2017

1 reference

9 October 2017

PubMed publication ID

9783718

1 reference