Documents
Is routine karyotyping required in prenatal samples with a molecular or metabolic referral?
Kooper, Pieters, Faas, Hoefsloot, Zondervan, Van, Smits
Documents
Array comparative genomic hybridization in prenatal diagnosis of first trimester pregnancies at high risk for chromosomal anomalies
Filges Isabel, Kang Anjeung, Klug Vanessa, Wenzel Friedel, Heinimann Karl, Tercanli Sevgi, Miny, Miny Peter
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Diagnóstico Prenatal Genético No Invasivo: Reflexión Bioética Sobre la Utilización del Diagnóstico Prenatal No Invasivo a Partir del Análisis de Ácidos Nucleicos Presentes en Sangre Periférica Materna (Noninvasive Prenatal Genetic Diagnosis: A Bioethical Reflection on the Use of Noninvasive Prenatal Diagnosis From the Analysis of Nucleic Acids Present in Maternal Peripheral Blood)
Fermín
Documents
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Diagnóstico Prenatal Genético No Invasivo: Reflexión Bioética Sobre la Utilización del Diagnóstico Prenatal No Invasivo a Partir del Análisis de Ácidos Nucleicos Presentes en Sangre Periférica Materna (Noninvasive Prenatal Genetic Diagnosis: A Bioethical Reflection on the Use of Noninvasive Prenatal Diagnosis From the Analysis of Nucleic Acids Present in Maternal Peripheral Blood)
Fermín
28 pages
Español
Documents
2D DIGE analysis of maternal plasma for potential biomarkers of Down Syndrome
Heywood, Madgett, Wang Darrell, Wallington Amanda, Hogg Julie, Mills Kevin, Avent
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