FMR1 CGG repeat expansion mutation detection and linked haplotype analysis for reliable and accurate preimplantation genetic diagnosis of fragile X syndrome.
- DOI
- 10.1017/erm.2017.10
- Published
- 2017 Jul 19
- Container
- Expert reviews in molecular medicine
- Publisher
- Not recorded
- Open access
- yes
Credibility signals
limited evidence Score 45/100 under policy 1.0.0. This is a metadata assessment, not a judgment of the paper's conclusions.
Show all credibility signals
- cautionDOI registered: No matching Crossref record was present in this response.
- cautionDOI resolves: No matching Crossref record was present in this response.
- not scoredDirectory of Open Access Journals: No matching DOAJ record was present in this response. No allow-list match; this is not evidence of low credibility.
- not scoredMEDLINE indexed: Not checked or no result supplied; no credibility inference made.
- not scoredOpenAlex core source: Not checked or no result supplied; no credibility inference made.
- not scoredKnown publisher allow-list: Not checked or no result supplied; no credibility inference made.
- not scoredROR affiliation: Not checked or no result supplied; no credibility inference made.
- not scoredRetraction Watch retraction: No retraction notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete.
- not scoredRetraction Watch expression of concern: No expression of concern notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete.
- not scoredRetraction Watch correction: No correction notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete.
- not scoredRetraction Watch reinstatement: No reinstatement notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete.
- supportingOpen access status: Normalized open-access status: open.
- not scoredPublication license: Not checked or no result supplied; no credibility inference made.
- not scoredPublication version: A publication version was supplied but is not scored.
- cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty.
Cite this work
BibTeX
@article{allodium:10.1017/erm.2017.10,
title = {FMR1 CGG repeat expansion mutation detection and linked haplotype analysis for reliable and accurate preimplantation genetic diagnosis of fragile X syndrome.},
author = {Rajan-Babu IS and Lian M and Cheah FSH and Chen M and Tan ASC and Prasath EB and Loh SF and Chong SS},
year = {2017},
journal = {Expert reviews in molecular medicine},
doi = {10.1017/erm.2017.10},
url = {https://doi.org/10.1017/erm.2017.10}
}RIS
TY - JOUR TI - FMR1 CGG repeat expansion mutation detection and linked haplotype analysis for reliable and accurate preimplantation genetic diagnosis of fragile X syndrome. AU - Rajan-Babu IS AU - Lian M AU - Cheah FSH AU - Chen M AU - Tan ASC AU - Prasath EB AU - Loh SF AU - Chong SS PY - 2017 JO - Expert reviews in molecular medicine DO - 10.1017/erm.2017.10 UR - https://doi.org/10.1017/erm.2017.10 ER -
APA
IS, R., M, L., FSH, C., M, C., ASC, T., EB, P., SF, L., & SS, C. (2017). FMR1 CGG repeat expansion mutation detection and linked haplotype analysis for reliable and accurate preimplantation genetic diagnosis of fragile X syndrome.. Expert reviews in molecular medicine. https://doi.org/10.1017/erm.2017.10
Source records
- pubmed · retrieved 2026-11-11T00:06:55.971Z
- europe-pmc · retrieved 2026-11-11T00:06:55.977Z