Whole-exome sequencing in patients with premature ovarian insufficiency: early detection and early intervention

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1757-2215

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Whole-exome sequencing in patients with premature ovarian insufficiency: early detection and early intervention ; volume:13 ; number:1 ; day:22 ; month:9 ; year:2020 ; pages:1-8 ; date:12.2020
Journal of ovarian research ; 13, Heft 1 (22.9.2020), 1-8, 12.2020

Creator: Liu, Hongli
Wei, Xiaoli
Sha, Yanwei
Liu, Wensheng
Gao, Haijie
Lin, Jin
Li, Youzhu
Tang, Yaling
Wang, Yifeng
Wang, Yanlong
Su, Zhiying

Contributor: SpringerLink (Online service)

DOI: 10.1186/s13048-020-00716-6

URN: urn:nbn:de:101:1-2020110921253248711199

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:23 AM CEST

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Associated

Liu, Hongli
Wei, Xiaoli
Sha, Yanwei
Liu, Wensheng
Gao, Haijie
Lin, Jin
Li, Youzhu
Tang, Yaling
Wang, Yifeng
Wang, Yanlong
Su, Zhiying
SpringerLink (Online service)

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Whole-exome sequencing in patients with premature ovarian insufficiency: early detection and early intervention

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Other Objects (12)

A novel EIF4ENIF1 mutation associated with a diminished ovarian reserve and premature ovarian insufficiency identified by whole-exome sequencing

Two siblings with early repolarization syndrome: clinical and genetic characterization by whole-exome sequencing

Early exploration of two candidate breast cancer susceptibility genes identified by whole-exome sequencing

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A maternal GOT1 novel variant associated with early-onset severe preeclampsia identified by whole-exome sequencing

Identification of novel candidate variants including COL6A6 polymorphisms in early-onset atopic dermatitis using whole-exome sequencing

Linkage analysis coupled with exome sequencing identified defects in gene ‘X’ causing premature ovarian insufficiency

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Comprehensive comparison of three commercial human whole-exome capture platforms

A novel EIF4ENIF1 mutation associated with a diminished ovarian reserve and premature ovarian insufficiency identified by whole-exome sequencing

Two siblings with early repolarization syndrome: clinical and genetic characterization by whole-exome sequencing

Early exploration of two candidate breast cancer susceptibility genes identified by whole-exome sequencing

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A maternal GOT1 novel variant associated with early-onset severe preeclampsia identified by whole-exome sequencing

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Linkage analysis coupled with exome sequencing identified defects in gene ‘X’ causing premature ovarian insufficiency

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Two siblings with early repolarization syndrome: clinical and genetic characterization by whole-exome sequencing

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A maternal GOT1 novel variant associated with early-onset severe preeclampsia identified by whole-exome sequencing

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