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Prenatal detection of a 3q29 microdeletion in a fetus with ventricular septum defect: A case report and literature review
RATIONALE: Chromosomal 3q deletion is a recurrent genomic alternation, which is rarely reported in clinic. PATIENT CONCERNS: A 27-year-old woman underwent amniocentesis for cytogenetic analysis and single nucleotide polymorphism (SNP) array analysis at 27 weeks of gestation, due to ventricular septu...
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| Publicat a: | Medicine (Baltimore) |
|---|---|
| Autors principals: | , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Lippincott Williams & Wilkins
2021
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7793333/ https://ncbi.nlm.nih.gov/pubmed/33429816 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MD.0000000000024224 |
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