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Prenatal diagnosis of a de novo tetrasomy 15q24.3‐25.3: Case report and literature review
BACKGROUND: Terminal duplication on chromosome 15q is a rare chromosomal variation. Affected individuals show similar features such as growth dysplasia or the development of frontal bossing, body deformities, facial abnormalities, and genitourinary or cardiovascular disorders. However, it is not yet...
Kaydedildi:
| Yayımlandı: | J Clin Lab Anal |
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| Asıl Yazarlar: | , , , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
John Wiley and Sons Inc.
2020
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7370735/ https://ncbi.nlm.nih.gov/pubmed/32185823 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jcla.23288 |
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