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Prenatal diagnosis of autosomal recessive Robinow syndrome using 3D ultrasound
This article hypothesizes that it is possible to detect and diagnose both the autosomal recessive and dominant forms prenatally using ultrasound. By focusing on the characteristic phenotypical presentation, the examinator is able to diagnose the syndrome prenatally, which is of clinical importance t...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Clin Case Rep |
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| Κύριοι συγγραφείς: | , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
John Wiley and Sons Inc.
2017
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5494388/ https://ncbi.nlm.nih.gov/pubmed/28680597 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ccr3.784 |
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