Detection of de novo genetic variants in Mayer–Rokitansky–Küster–Hauser syndrome by whole genome sequencing
Hongxin Pan, Guangnan Luo, Shengqing Wan, Chenglu Qin, Jie Tang, Meng Zhang, Min Du, Keke Xu, Jin-qiu Shi
- ISSN / E-ISSN
- — / —
- DOI
- 10.1016/j.eurox.2019.100089 ↗
- Volume · Issue · Pages
- 4 · — · 100089-100089
- Publisher
- Elsevier Ireland Ltd
- Article URL
- https://doi.org/10.1016/j.eurox.2019.100089 ↗
- Article details
- Unverified
Publication date (each date has its type and source)
02 Aug 2019
OpenAlex publication date · source: OpenAlex
| Type | Date | Source |
|---|---|---|
| OpenAlex publication date | 02 Aug 2019 | OpenAlex |
Keywords (as given): de novo mutations; single nucleotide variants; small insertions and deletions; copy number alterations; structural variants; PIK3CD; SLC4A10; TNK2; BAZ2B; promoter polymorphism; 3'UTR variant; candidate genes; case-parent trios
HEC Status at Publication Not the journal's current status
HEC Status at PublicationNot conclusive
Historical status could not be conclusively determined.
- HEC status cannot be determined for this date: no HEC list is recorded as in effect on it.
Best available information, not a definitive status: HEC status cannot be determined for this date: no HEC list is recorded as in effect on it.
- Journal
- European Journal of Obstetrics and Gynecology and Reproductive Biology: X
- Publication date used
- 02 Aug 2019 (OpenAlex publication date)
- Applicable HEC period
- None recorded for this date
- Category
- —
- Recognition status
- Unknown (NO_PERIOD_FOR_DATE)
- Source
- —
- Verification status
- Not available
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