诊断原发性卵巢功能不全（POI）的基因组学：大门是敞开的，但道路仍有待铺设。

IF 6 1区医学 Q1 OBSTETRICS & GYNECOLOGY

Human reproduction Pub Date : 2025-04-28 DOI:10.1093/humrep/deaf084

Omar F Ammar,George Liperis,Kashish Sharma,Zoya E Ali,Patricia Diaz-Gimeno,Filippo Zambelli,Martine A Gould,Vikram Talaulikar,Juan J Fraire-Zamora

引用次数: 0

摘要

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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Genomics in diagnosing primary ovarian insufficiency (POI): the door is open, but the path is still to be paved.

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来源期刊

Human reproduction 医学-妇产科学

CiteScore

10.90

自引率

6.60%

发文量

1369

审稿时长

1 months

期刊介绍： Human Reproduction features full-length, peer-reviewed papers reporting original research, concise clinical case reports, as well as opinions and debates on topical issues. Papers published cover the clinical science and medical aspects of reproductive physiology, pathology and endocrinology; including andrology, gonad function, gametogenesis, fertilization, embryo development, implantation, early pregnancy, genetics, genetic diagnosis, oncology, infectious disease, surgery, contraception, infertility treatment, psychology, ethics and social issues.