(Q33595805)

28 July 2017

title

Prenatal diagnosis of a hypermethylated full fragile X mutation in chorionic villi of a male fetus (English)

1 reference

28 July 2017

1 reference

Suzumori K

1

1 reference

28 July 2017

Yamauchi M

2

1 reference

28 July 2017

Seki N

3

1 reference

28 July 2017

Kondo I

4

1 reference

28 July 2017

Hori T

5

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 September 1993

1 reference

Journal of Medical Genetics

28 July 2017

published in

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28 July 2017

volume

30

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28 July 2017

issue

9

1 reference

28 July 2017

page(s)

785-787

1 reference

Heritable unstable DNA sequences and hypermethylation associated with fragile X syndrome in Japanese families.

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=1016539

Prenatal diagnosis of fragile X syndrome by direct detection of the unstable DNA sequence

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016539

Molecular genetics of the fragile-X syndrome: a novel type of unstable mutation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016539

Rapid preparation of diagnostic probes for the fragile X syndrome by direct PCR amplification of human chromosomal DNA

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016539

DNA methylation represses FMR-1 transcription in fragile X 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=1016539

Analysis of full fragile X mutations in fetal tissues and monozygotic twins indicate that abnormal methylation and somatic heterogeneity are established early in development

21 June 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/8411077

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Prenatal diagnosis of fragile X syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/8411077

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JMG.30.9.785

1 reference

28 July 2017

1 reference

28 July 2017

1 reference