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Prenatal diagnosis of factor X deficiency using a combination of direct mutation detection and linkage analysis with an intragenic single nucleotide polymorphism
Authors:Rodney Camire  Ruth Ann Denchy  George A Day III  Patricia Lanzano  Sujit Sheth  Stephen Brown
Institution:1. Department of Pediatrics, The University of Pennsylvania, School of Medicine and The Children's Hospital of Philadelphia, Philadelphia, USA;2. Department of Obstetrics and Gynecology, Columbia University, College of Physicians and Surgeons, New York, USA;3. Department of Pediatrics, Columbia University, College of Physicians and Surgeons, New York, USA
Abstract:
Keywords:factor X  linkage  SNP  coagulation  CVS
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