GB201718620D0 - Method of detecting a fetal chromosomal abnormality - Google Patents
Method of detecting a fetal chromosomal abnormalityInfo
- Publication number
- GB201718620D0 GB201718620D0 GBGB1718620.6A GB201718620A GB201718620D0 GB 201718620 D0 GB201718620 D0 GB 201718620D0 GB 201718620 A GB201718620 A GB 201718620A GB 201718620 D0 GB201718620 D0 GB 201718620D0
- Authority
- GB
- United Kingdom
- Prior art keywords
- detecting
- chromosomal abnormality
- fetal chromosomal
- fetal
- abnormality
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
- C12Q1/6876—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
- C12Q1/6883—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB1718620.6A GB201718620D0 (en) | 2017-11-10 | 2017-11-10 | Method of detecting a fetal chromosomal abnormality |
PCT/GB2018/053255 WO2019092438A1 (en) | 2017-11-10 | 2018-11-12 | Method of detecting a fetal chromosomal abnormality |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB1718620.6A GB201718620D0 (en) | 2017-11-10 | 2017-11-10 | Method of detecting a fetal chromosomal abnormality |
Publications (1)
Publication Number | Publication Date |
---|---|
GB201718620D0 true GB201718620D0 (en) | 2017-12-27 |
Family
ID=60788314
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GBGB1718620.6A Ceased GB201718620D0 (en) | 2017-11-10 | 2017-11-10 | Method of detecting a fetal chromosomal abnormality |
Country Status (2)
Country | Link |
---|---|
GB (1) | GB201718620D0 (en) |
WO (1) | WO2019092438A1 (en) |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US10095831B2 (en) * | 2016-02-03 | 2018-10-09 | Verinata Health, Inc. | Using cell-free DNA fragment size to determine copy number variations |
-
2017
- 2017-11-10 GB GBGB1718620.6A patent/GB201718620D0/en not_active Ceased
-
2018
- 2018-11-12 WO PCT/GB2018/053255 patent/WO2019092438A1/en active Application Filing
Also Published As
Publication number | Publication date |
---|---|
WO2019092438A1 (en) | 2019-05-16 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
AT | Applications terminated before publication under section 16(1) |