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| Status |
Public on Jan 24, 2023 |
| Title |
Genetic analysis, ultrasound phenotype, and pregnancy outcome of fetuses with Xp22.33 or Yp11.32 microdeletion |
| Organism |
Homo sapiens |
| Experiment type |
Genome variation profiling by SNP array
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| Summary |
The phenotypes of Xp22.33 or Yp11.32 microdeletions containing short-stature homeobox (SHOX) gene have been extensively described in adults and children, however, few have been reported in prenatal fetuses.
We analyzed the prenatal ultrasound phenotype and pregnancy outcomes of fetuses with Xp22.33 or Yp11.32 microdeletion containing SHOX gene to improve the understanding, diagnosis, and monitoring of the disease in the fetal period.
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| Overall design |
Chromosomal analysis and chromosomal microarray analysis (CMA) were performed
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| Contributor(s) |
Cai M, Huang H |
| Citation missing |
Has this study been published? Please login to update or notify GEO. |
| Submission date |
Jan 19, 2023 |
| Last update date |
Jan 27, 2023 |
| Contact name |
Hailong Huang |
| Organization name |
Fujian Maternity and Child Health Hospital
|
| Street address |
No.18 Daoshan Road, Gulou District
|
| City |
Fuzhou |
| State/province |
Fujian |
| ZIP/Postal code |
350001 |
| Country |
China |
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| Platforms (1) |
| GPL18637 |
[CytoScan750K_Array] Affymetrix CytoScan 750K Array |
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| Samples (5)
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| Relations |
| BioProject |
PRJNA925455 |
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