Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Prevalence of the FMR1 mutation in Taiwan assessed by large-scale screening of newborn boys and analysis of DXS548-FRAXAC1 haplotype.

American journal of medical genetics. Part A - 15 Feb 2005

Tzeng Ching-Cherng, Tsai Li-Ping, Hwu Wuh-Liang, Lin Shio-Jean, Chao Mei-Chyn, Jong Yuh-Jyh, Chu Shao-Yin, Chao Wei-Chen, Lu Chin-Li

Abstract excerpt

If carrier women could be identified in time and take appropriate measures, fragile X syndrome (FXS) can be prevented. Wide screening of women to be or in their early pregnancy was considered a good approach to identify carriers without misdetection. Nevertheless, we argued against the cost-effec...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Chromosomes, Human, X
Share to Fragile X Mental Retardation Protein

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Fragile X Syndrome

Share to Nerve Tissue Proteins

Share to Prevalence

Share to RNA-Binding Proteins

Share to Taiwan

Share to Trinucleotide Repeats

Source

Identifiers

PMID: 15637705
DOI: 10.1002/ajmg.a.30528

Genes

FMR1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-15637705-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Prevalence of the FMR1 mutation in Taiwan assessed by large-scale screening of newborn boys and analysis of DXS548-FRAXAC1 haplotype.PMID 15637705Read ↗

Pilot fragile X screening in normal population of Taiwan.Semantic proximity Read ↗

A 15-year-long Southern blotting analysis of FMR1 to detect female carriers and for prenatal diagnosis of fragile X syndrome in Taiwan.Semantic proximity Read ↗

Fragile X syndrome carrier screening in pregnant women in Chinese Han population.Semantic proximity Read ↗

Development of Chinese genetic reference panel for Fragile X Syndrome and its application to the screen of 10,000 Chinese pregnant women and women planning pregnancy.Semantic proximity Read ↗

FMR1 allele frequencies in 51,000 newborns: a large-scale population study in China.Semantic proximity Read ↗

Identification of fragile X pre-mutation carriers in the Chinese obstetric population using a robust FMR1 polymerase chain reaction assay: implications for screening and prenatal diagnosis.Semantic proximity Read ↗

Original article pilot screening for fragile X carrier in pregnant women of southern Taiwan.Semantic proximity Read ↗

Frequency of the fragile X syndrome in Chinese mentally retarded populations is similar to that in Caucasians.Semantic proximity Read ↗

Allele distribution at the FMR1 locus in the general Chinese population.Semantic proximity Read ↗

Population-based Carrier Screening and Prenatal Diagnosis of Fragile X Syndrome in East Asian PopulationsSemantic proximity Read ↗

FMR1 gene mutations in patients with fragile X syndrome and obligate carriers: 30 years of experience in Chile.Semantic proximity Read ↗

Fragile X syndrome screening in pregnant women and women planning pregnancy shows a remarkably high FMR1 premutation prevalence in the Balearic Islands.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.