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Prenatal diagnosis of skeletal dysplasia due to FGFR3 gene mutations: a 9-year experience
Journal of Assisted Reproduction and Genetics, 10/02/09
Fenollar–Cortes M et al. – Molecular studies in ongoing pregnancies are indicated in cases with an affected parent, a family history with positive molecular studies (maternal anxiety), and when the US finding demonstrates micromelia with a hypoplastic thorax. A protocol for tissues of abortuses should include an X–ray, pathologic anatomy, and genetic studies.
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Obstetric analgesia: a comparison of patient-controlled meperidine, remifentanil, and fentanyl in labour
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