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  • Print publication year: 2018
  • Online publication date: February 2018

Chapter 21 - Genetic Counseling and Prenatal Diagnosis of Congenital Bleeding Disorders

from Section 7 - Hemorrhagic Disorders
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12.Payne, AB, Bean, CJ, Hooper, WC, Miller, CH. Utility of multiplex ligation-dependent probe amplification (MLPA) for hemophilia mutation screening. Journal of Thrombosis and Haemostasis 2012; 10: 19511954.
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15.Lee, C, Chi, C, Pavord, SR et al. The obstetric and gynecological management of women with inherited bleeding disorders – review of guidelines produced by a taskforce of UK Hemophilia Center Doctors’ Organization. Hemophilia 2006; 12: 301336.
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19.Bustamente-Aragones, A, Rodriguez de Alba, M, Gonzalez-Gonzalez, C et al. Foetal sex determination in maternal blood from the seventh week of gestation and its role in diagnosing hemophilia in the foetuses of female carriers. Hemophilia 2008; 14: 593598.
20.RCOG. Amniocentesis and Chorionic Villous Sampling. Green-Top Guideline No. 8. London: Royal College of Obstetricians and Gynecologists; 2010.
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22.Cutler, J, Chappell, LC, Kyle, P, Madan, B. Third trimester amniocentesis for diagnosis of inherited bleeding disorders prior to delivery. Hemophilia 2013; 19: 904907.
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