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Prenatal diagnosis of skeletal dysplasia due to FGFR3 gene mutations: a 9-year experience
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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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Nitrofurantoin transport by placental choriocarcinoma JAr cells: involvement of BCRP, OATP2B1 and other MDR transporters
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Higher interleukin-18 and mannose-binding lectin are present in uterine lumen of patients with unexplained infertility
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Evaluation of endometrial thickness with transvaginal ultrasonography and histopathology in premenopausal women with abnormal vaginal bleeding
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