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The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data
The updated HPO database is described, which provides annotations of 7,278 human hereditary syndromes listed in OMIM, Orphanet and DECIPHER to classes of the HPO, allowing integration of existing datasets and interoperability with multiple biomedical resources.
Chromosomal microarray versus karyotyping for prenatal diagnosis.
In the context of prenatal diagnostic testing, chromosomal microarray analysis identified additional, clinically significant cytogenetic information as compared with karyotyping and was equally efficacious in identifying aneuploidies and unbalanced rearrangements but did not identify balanced translocations and triploidy.
Maternal Morbidity Associated With Multiple Repeat Cesarean Deliveries
The number of intended pregnancies should be considered during counseling regarding elective repeat cesarean operation versus a trial of labor and when debating the merits of elective primary cESarean delivery.
Prevention of recurrent preterm delivery by 17 alpha-hydroxyprogesterone caproate
Preterm delivery before 37 completed weeks gestation remains the major factor influencing infant mortality in developed countries. Women who have had a spontaneous preterm delivery are at much higher
Maternal and perinatal outcomes associated with a trial of labor after prior cesarean delivery.
A trial of labor after prior cesarean delivery is associated with a greater perinatal risk than is elective repeated cesAREan delivery without labor, although absolute risks are low.
Development of a Nomogram for Prediction of Vaginal Birth After Cesarean Delivery
A predictive nomogram, which incorporates six variables easily ascertainable at the first prenatal visit, has been developed that allows the determination of a patient-specific chance for successful VBAC for those women who undertake trial of labor.
Expanded carrier screening in reproductive medicine-points to consider: a joint statement of the American College of Medical Genetics and Genomics, American College of Obstetricians and
The Perinatal Quality Foundation and the American College of Medical Genetics and Genomics, in association with the American College of Obstetricians and Gynecologists, the Society for Maternal-Fetal