|
| Status |
Public on Jul 21, 2025 |
| Title |
Genetic etiology and phenotypic characteristics of fetuses with 11q deletion (11q23.3-q25) syndrome |
| Organism |
Homo sapiens |
| Experiment type |
Genome variation profiling by SNP array
|
| Summary |
To investigate the clinical phenotype, genetic etiology, and diagnosis of 11q deletion (11q-) syndrome.
The differences and severity of fetal phenotypes may depend on the types and quantities of functional genes contained in fragments of different sizes.
|
| |
|
| Overall design |
In this study, pregnant women were selected from prenatal testing in Longgang Maternal and Child Health Hospital of Shenzhen. After screening for prenatal serological analysis, noninvasive prenatal genetic testing screening (NIPS), chromosome karyotype analysis, and chromosome microarray analysis (CMA), 4 pregnant women diagnosed with 11q- syndrome were selected for retrospective analysis.
|
| |
|
| Contributor(s) |
Zhang T, Liu W |
| Citation missing |
Has this study been published? Please login to update or notify GEO. |
| |
| Submission date |
Jan 17, 2025 |
| Last update date |
Jul 22, 2025 |
| Contact name |
Tong Zhang |
| E-mail(s) |
zt0720zt@126.com
|
| Phone |
13048828750
|
| Organization name |
Longgang District Maternity & Child Healthcare Hospital of Shenzhen City
|
| Street address |
Longgang District Maternity & Child Healthcare Hospital of Shenzhen City
|
| City |
Shenzhen |
| ZIP/Postal code |
518172 |
| Country |
China |
| |
|
| Platforms (2) |
| GPL18637 |
[CytoScan750K_Array] Affymetrix CytoScan 750K Array |
| GPL32641 |
[CytoScanOptima_Array] Affymetrix CytoScan Optima Array |
|
| Samples (4)
|
|
| Relations |
| BioProject |
PRJNA1212132 |
Less...
More...