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Investigation of the molecular genetic causes of non-syndromic primary ovarian ınsufficiency by next generation sequencing analysis.

Archives of endocrinology and metabolism - 17 Nov 2023

Er Eren, Aşıkovalı Semih, Özışık Hatice, Sağsak Elif, GÖkşen Damla, Onay Hüseyin, Saygılı Füsun, Darcan Şükran, Özen Samim

Abstract excerpt

Objective: The aim of this study is to investigate the molecular genetic causes of non-syndromic primary ovarian insufficiency (POI) cases with the gene panel basedon next generation sequencing analysis and to establish the relationship between genotype and phenotype. Materials and methods: Twenty three cases aged 14-40 years followed up with POI were included. Patients with a karyotype of 46, XX, primary or...

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Identifiers

PMID: 37988663
DOI: 10.20945/2359-4292-2022-0475
PMCID: PMC10916837

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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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