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Preimplantation Genetic Diagnosis for Severe Albright Hereditary Osteodystrophy
Context: Preimplantation genetic diagnosis (PGD) enables the selection of embryos without mutations for implantation and has not been described to our knowledge for mutations in GNAS. Phocomelia in a patient with Albright hereditary osteodystrophy (AHO) has also not been previously described. Object...
Αποθηκεύτηκε σε:
| Κύριοι συγγραφείς: | , , , |
|---|---|
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
The Endocrine Society
2008
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2266954/ https://ncbi.nlm.nih.gov/pubmed/18089698 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jc.2007-2040 |
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