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Article

Ethical Dilemmas Linked to Fragile X Testing of Minors-a Preliminary Survey Among Professionals.

Journal of molecular neuroscience : MN - 1 Feb 2020

Gabis Lidia V, Shefer Shahar, Raas-Rothschild Annick

Abstract excerpt

Asymptomatic female carriers of the FMR1 premutation at childbearing age have been mostly identified through prenatal genetic testing, which is routinely proposed in Israel. During the last few years, a premutation phenotype in males and females has been defined-FXAND, including neuropsychiatric disorder, learning difficulties, endocrine dysfunction, and premature ovarian failure. So when a family at risk is...

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Share to Fragile X Mental Retardation Protein
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 31993931
DOI: 10.1007/s12031-019-01445-2

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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